Other products from "ORTHOSOFT INC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024304536 20-8000-010-30 20-8000-010-30 HAW Neurological Stereotaxic Instrument 2 NA
2 00889024304529 20-8000-010-29 20-8000-010-29 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
3 00889024304512 20-8000-010-28 20-8000-010-28 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
4 00889024304505 20-8000-010-27 20-8000-010-27 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
5 00889024304499 20-8000-010-26 20-8000-010-26 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
6 00889024304482 20-8000-010-25 20-8000-010-25 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
7 00889024304475 20-8000-010-24 20-8000-010-24 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
8 00889024304468 20-8000-010-23 20-8000-010-23 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
9 00889024304451 20-8000-010-22 20-8000-010-22 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
10 00889024304437 20-8000-010-20 20-8000-010-20 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
11 00889024304420 20-8000-010-19 20-8000-010-19 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
12 00889024304413 20-8000-010-18 20-8000-010-18 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
13 00889024304406 20-8000-010-17 20-8000-010-17 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
14 00889024304376 20-8000-010-14 20-8000-010-14 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
15 00889024304369 20-8000-010-13 20-8000-010-13 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
16 00889024304352 20-8000-010-12 20-8000-010-12 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
17 00889024304345 20-8000-010-11 20-8000-010-11 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
18 00889024304321 20-8000-010-09 20-8000-010-09 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
19 00889024304314 20-8000-010-07 20-8000-010-07 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
20 00889024304291 20-8000-010-01 20-8000-010-01 HAW,OLO Neurological Stereotaxic Instrument,Orthopedic Stereotaxic Instrument 2 NA
21 00889024305304 20-8011-020-00 20-8011-020-00 OLO Orthopedic Stereotaxic Instrument 2 NA
22 00889024305298 20-8011-019-00 20-8011-019-00 OLO Orthopedic Stereotaxic Instrument 2 NA
23 00889024305281 20-8011-018-00 20-8011-018-00 OLO Orthopedic Stereotaxic Instrument 2 NA
24 00889024305380 20-8011-028-50 20-8011-028-50 OLO Orthopedic Stereotaxic Instrument 2 NA
25 00889024305373 20-8011-028-00 20-8011-028-00 OLO Orthopedic Stereotaxic Instrument 2 NA
26 00889024305366 20-8011-027-50 20-8011-027-50 OLO Orthopedic Stereotaxic Instrument 2 NA
27 00889024305359 20-8011-027-00 20-8011-027-00 OLO Orthopedic Stereotaxic Instrument 2 NA
28 00889024305342 20-8011-026-00 20-8011-026-00 OLO Orthopedic Stereotaxic Instrument 2 NA
29 00889024305335 20-8011-025-00 20-8011-025-00 OLO Orthopedic Stereotaxic Instrument 2 NA
30 00889024492714 20-8011-013-01 OLO Orthopedic Stereotaxic Instrument 2 NA
31 00889024492707 20-8000-000-21 OLO Orthopedic Stereotaxic Instrument 2 NA
32 00889024492691 20-8000-000-15 OLO Orthopedic Stereotaxic Instrument 2 NA
33 00889024305311 20-8011-021-00 20-8011-021-00 OLO Orthopedic Stereotaxic Instrument 2 NA
34 00889024305274 20-8011-017-00 20-8011-017-00 OLO Orthopedic Stereotaxic Instrument 2 NA
35 00889024492660 20-8000-020-27 HAW Neurological Stereotaxic Instrument 2 NA
36 00889024479012 20-8000-080-11 OLO Orthopedic Stereotaxic Instrument 2 NA
37 00889024479005 20-8000-080-10 OLO Orthopedic Stereotaxic Instrument 2 NA
38 00889024305267 20-8011-013-00 20-8011-013-00 OLO Orthopedic Stereotaxic Instrument 2 NA
39 00889024304840 20-8000-020-10 20-8000-020-10 HAW Neurological Stereotaxic Instrument 2 NA
40 00889024305410 20-8011-042-00 20-8011-042-00 OLO Orthopedic Stereotaxic Instrument 2 NA
41 00889024304888 20-8000-020-14 20-8000-020-14 HAW Neurological Stereotaxic Instrument 2 NA
42 00889024304871 20-8000-020-13 20-8000-020-13 HAW Neurological Stereotaxic Instrument 2 NA
43 00889024304598 20-8000-010-37 20-8000-010-37 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
44 00889024305564 20-8014-014-00 20-8014-014-00 OOG,MBH,JWH Knee Arthroplasty Implantation System,Prosthesis, Knee, Patello/Femorotibial, Se Knee Arthroplasty Implantation System,Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 NA
45 00889024304574 20-8000-010-35 20-8000-010-35 OLO,HAW Orthopedic Stereotaxic Instrument,Neurological Stereotaxic Instrument 2 NA
46 00889024305526 20-8011-070-03 20-8011-070-03 HAW Neurological Stereotaxic Instrument 2 NA
47 00889024305519 20-8011-070-02 20-8011-070-02 HAW Neurological Stereotaxic Instrument 2 NA
48 00889024305465 20-8011-056-52 20-8011-056-52 OLO Orthopedic Stereotaxic Instrument 2 NA
49 00889024304857 20-8000-020-11 20-8000-020-11 HAW Neurological Stereotaxic Instrument 2 NA
50 00889024305458 20-8011-056-51 20-8011-056-51 OLO Orthopedic Stereotaxic Instrument 2 NA
Other products with the same Product Codes "LLZ, OLO"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 04546540392114 6007-011-000 6007-011-000 POINTER, STRAIGHT NA STRYKER LEIBINGER GMBH & CO. KG
2 04546540392107 6007-010-000 6007-010-000 PATIENT TRACKER, BLUE NA STRYKER LEIBINGER GMBH & CO. KG
3 04546540392084 6007-005-000 6007-005-000 PATIENT TRACKER, GREEN NA STRYKER LEIBINGER GMBH & CO. KG
4 04546540391957 6003-100-100 6003-100-100 SCREWDRIVER NA STRYKER LEIBINGER GMBH & CO. KG
5 04546540391773 6007-460-000 6007-460-000 ANCHORING PIN 60MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
6 04546540391766 6007-455-000 6007-455-000 ANCHORING PIN 55MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
7 04546540391759 6007-445-000 6007-445-000 ANCHORING PIN 45MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
8 04546540391742 6007-435-000 6007-435-000 ANCHORING PIN 35MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
9 04546540391735 6007-425-000 6007-425-000 ANCHORING PIN 25MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
10 04546540391728 6007-420-000 6007-420-000 ANCHORING PIN 20MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
11 04546540373007 6007-550-000 6007-550-000 ANCHORING PIN 50MM/5MM NA STRYKER LEIBINGER GMBH & CO. KG
12 04546540372994 6007-540-000 6007-540-000 ANCHORING PIN 40MM/5MM NA STRYKER LEIBINGER GMBH & CO. KG
13 04546540372987 6007-530-000 6007-530-000 ANCHORING PIN 30MM/5MM NA STRYKER LEIBINGER GMBH & CO. KG
14 04546540372970 6007-450-000 6007-450-000 ANCHORING PIN 50MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
15 04546540372963 6007-440-000 6007-440-000 ANCHORING PIN 40MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
16 04546540372956 6007-430-000 6007-430-000 ANCHORING PIN 30MM/4MM NA STRYKER LEIBINGER GMBH & CO. KG
17 04546540361011 6003-100-020 6003-100-020 ADJUSTMENT COMPONENT NA STRYKER LEIBINGER GMBH & CO. KG
18 04546540246028 6003-011-000 6003-011-000 POINTER, KNEE NAVIGATION NA STRYKER LEIBINGER GMBH & CO. KG
19 04546540246011 6003-010-000 6003-010-000 FEMORAL TRACKER NA STRYKER LEIBINGER GMBH & CO. KG
20 04546540246004 6003-005-000 6003-005-000 TIBIAL/PELVIC TRACKER NA STRYKER LEIBINGER GMBH & CO. KG
21 04546540245984 6002-050-000 6002-050-000 ROTATIONAL NAVIGATION ADAPTER NA STRYKER LEIBINGER GMBH & CO. KG
22 04546540245045 6000-006-000 6000-006-000 INSTRUMENT BATTERY NA STRYKER LEIBINGER GMBH & CO. KG
23 04546540245038 6000-005-000 6000-005-000 UNIVERSAL TRACKER NA STRYKER LEIBINGER GMBH & CO. KG
24 04546540012982 6003-100-090 6003-100-090 TRACKER ADAPTER NA STRYKER LEIBINGER GMBH & CO. KG
25 04540217011469 502-24400-12 DAR-8000i SHIMADZU CORPORATION
26 04540217011452 502-24400-11 DAR-8000i SHIMADZU CORPORATION
27 04260648620022 2021 (Build 1920) Ashvins MEDICALCOMMUNICATIONS GMBH
28 04260648620015 2.5 Ashvins variant HEYEX 2 / HEYEX PACS MEDICALCOMMUNICATIONS GMBH
29 04260648620008 Ashvins 2020 Ashvins variant Diagnostic Workstation, Ashvins variant Image & Web Management MEDICALCOMMUNICATIONS GMBH
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31 04260632470022 5.2 Version 5.2 includes all minor versions and patch levels of 5.2 JiveX VISUS HEALTH IT GMBH
32 04260632470015 5.1 Version 5.1 includes all minor versions and patch levels of 5.1 JiveX VISUS HEALTH IT GMBH
33 04260583190017 20100131 Surgical Base System BRAINLAB AG
34 04260521365019 3.0 Galway exoplan is a medical software, intended to support the pre-operative planning of exoplan is a medical software, intended to support the pre-operative planning of dental implants using the visualization of the implant placement within images of the patient’s anatomy. The process is based on CT/CBCT data sets originating from other medical devices, and can be supported by optical scan(s) of the patient’s anatomy as well as a virtual prosthetic proposal. exoplan allows the design of surgical guides to support the placement of endosseous dental implants in guided surgery. The design of surgical guides is based on 3D surface data representing the preoperative situation and approved implant positions. Alternatively, instead of optical surface data a second CBCT/CT dataset can be used. The software exports the planning and design results as geometrical data and a digital 3D model of the surgical guide to support the manufacture of a separate physical product.exoplan does not extend or change indications of dental implants. Usage of a surgical guide designed with the software does not change the necessary due diligence required compared to conventional (non-guided) surgery.The software is intended to be used only by dental professionals with sufficient medical training in dental implantology and surgical dentistry in office environments suitable for reading diagnostic dental DICOM data sets. exoplan shall not be used for any purpose other than planning dental implant placement or design of surgical guides. exoplan EXOCAD GMBH
35 04260521365002 2.3 Matera exoplan is a medical software, intended to support the pre-operative planning of exoplan is a medical software, intended to support the pre-operative planning of dental implants using the visualization of the implant placement within images of the patient’s anatomy. The process is based on CT/CBCT data sets originating from other medical devices, and can be supported by optical scan(s) of the patient’s anatomy as well as a virtual prosthetic proposal.exoplan allows the design of surgical guides to support the placement of endosseous dental implants in guided surgery. The design of surgical guides is based on 3D surface data representing the preoperative situation and approved implant positions.The software exports the planning and design results as geometrical data and a digital 3D model of the surgical guide to support the manufacture of a separate physical product.exoplan does not extend or change indications of dental implants. Usage of a surgical guide designed with the software does not change the necessary due diligence required compared to conventional (non-guided) surgery.The software is intended to be used only by dental professionals with sufficient medical training in dental implantology and surgical dentistry in office environments suitable for reading diagnostic dental DICOM data sets. exoplan shall not be used for any purpose other than planning dental implant placement or design of surgical guides. exoplan EXOCAD GMBH
36 04260495880389 3.8.0 The product mint Lesion helps qualified radiologists with the image-based diagno The product mint Lesion helps qualified radiologists with the image-based diagnosis and treatment response assessment of oncological diseases. Fields of application are radiological diagnosis and follow-up examinations in oncology, as well as clinical or pharmaceutical drug trials across a defined group of patients.mint Lesion implements various radiological guidelines and response evaluation criteria, such as RECIST (Response Evaluation Criteria In Solid Tumors). This also includes the assessment of the stage of oncological disease (staging) and the objective response to therapy (e.g. timepoint response / overall response). The timepoint response is an empirical measure to evaluate therapy success according to the response criteria in use. It is mainly used to assess patient cohorts in the course of clinical trials of novel therapy agents. The timepoint response may differ from a radiological assessment of response to therapy and must not be used as a surrogate.mint Lesion allows for the documentation of size and assessment of changes in size of solid tumors described by the respective criteria that are monitored by means of radiological imaging (computed tomography (CT), magnetic resonance imaging (MRI), nuclear medicine (PET, NM), digital radiography (XR, CR)).mint Lesion follows the typical workflow of follow-up examinations, from assessment to reporting, and enables the integration of a clinical-radiological software environment (PACS, Picture Archiving and Communication System). Assessment results can be exported into different electronical formats and processed further by other applications. mintLesion™ MINT MEDICAL GMBH
37 04260495880372 3.7.0 The product mint Lesion helps qualified radiologists with the image-based diagno The product mint Lesion helps qualified radiologists with the image-based diagnosis and treatment response assessment of oncological diseases. Fields of application are radiological diagnosis and follow-up examinations in oncology, as well as clinical or pharmaceutical drug trials across a defined group of patients. mint Lesion implements various radiological guidelines and response evaluation criteria, such as RECIST (Response Evaluation Criteria In Solid Tumors). This also includes the assessment of the stage of oncological disease (staging) and the objective response to therapy (e.g. timepoint response / overall response). The timepoint response is an empirical measure to evaluate therapy success according to the response criteria in use. It is mainly used to assess patient cohorts in the course of clinical trials of novel therapy agents. The timepoint response may differ from a radiological assessment of response to therapy and must not be used as a surrogate. mint Lesion allows for the documentation of size and assessment of changes in size of solid tumors described by the respective criteria that are monitored by means of radiological imaging (computed tomography (CT), magnetic resonance imaging (MRI), nuclear medicine (PET, NM), digital radiography (XR, CR)). mint Lesion follows the typical workflow of follow-up examinations, from assessment to reporting, and enables the integration of a clinical-radiological software environment (PACS, Picture Archiving and Communication System). Assessment results can be exported into different electronical formats and processed further by other applications. mintLesion® MINT MEDICAL GMBH
38 04260495880365 3.6.0 The product mint Lesion helps qualified radiologists with the image-based diagno The product mint Lesion helps qualified radiologists with the image-based diagnosis and treatment response assessment of oncological diseases. Fields of application are radiological diagnosis and follow-up examinations in oncology, as well as clinical or pharmaceutical drug trials across a defined group of patients. mint Lesion implements various radiological guidelines and response evaluation criteria, such as RECIST (Response Evaluation Criteria In Solid Tumors). This also includes the assessment of the stage of oncological disease (staging) and the objective response to therapy (e.g. timepoint response / overall response). The timepoint response is an empirical measure to evaluate therapy success according to the response criteria in use. It is mainly used to assess patient cohorts in the course of clinical trials of novel therapy agents. The timepoint response may differ from a radiological assessment of response to therapy and must not be used as a surrogate. mint Lesion allows for the documentation of size and assessment of changes in size of solid tumors described by the respective criteria that are monitored by means of radiological imaging (computed tomography (CT), magnetic resonance imaging (MRI), nuclear medicine (PET, NM), digital radiography (XR, CR)). mint Lesion follows the typical workflow of follow-up examinations, from assessment to reporting, and enables the integration of a clinical-radiological software environment (PACS, Picture Archiving and Communication System). Assessment results can be exported into different electronical formats and processed further by other applications. mintLesion® MINT MEDICAL GMBH
39 04260495880358 3.5.0 The product mint Lesion helps qualified radiologists with the image-based diagno The product mint Lesion helps qualified radiologists with the image-based diagnosis and treatment response assessment of oncological diseases. Fields of application are radiological diagnosis and follow-up examinations in oncology, as well as clinical or pharmaceutical drug trials across a defined group of patients. mint Lesion implements various radiological guidelines and response evaluation criteria, such as RECIST (Response Evaluation Criteria In Solid Tumors). This also includes the assessment of the stage of oncological disease (staging) and the objective response to therapy (e.g. timepoint response / overall response). The timepoint response is an empirical measure to evaluate therapy success according to the response criteria in use. It is mainly used to assess patient cohorts in the course of clinical trials of novel therapy agents. The timepoint response may differ from a radiological assessment of response to therapy and must not be used as a surrogate. mint Lesion allows for the documentation of size and assessment of changes in size of solid tumors described by the respective criteria that are monitored by means of radiological imaging (computed tomography (CT), magnetic resonance imaging (MRI), nuclear medicine (PET, NM), digital radiography (XR, CR)). mint Lesion follows the typical workflow of follow-up examinations, from assessment to reporting, and enables the integration of a clinical-radiological software environment (PACS, Picture Archiving and Communication System). Assessment results can be exported into different electronical formats and processed further by other applications. mintLesion® MINT MEDICAL GMBH
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