Duns Number:134614411
Device Description: Sterile needle guide with (14 x 91.5cm) telescopically-folded CIV-Flex™ cover
Catalog Number
610-692
Brand Name
Ultra-Pro II™ Needle Guide
Version/Model Number
610-692
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 15, 2019
Issuing Agency
In GS1
MRI safety Status
Labeling does not contain MRI Safety Information
Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)
-
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K093713,K093713
Product Code
ITX
Product Code Name
Transducer, ultrasonic, diagnostic
Public Device Record Key
d030e0d4-e641-47c9-aad8-f4066a318180
Public Version Date
June 17, 2022
Public Version Number
8
DI Record Publish Date
August 22, 2017
Package DI Number
00841436103992
Quantity per Package
24
Contains DI Package
10841436103999
Package Discontinue Date
October 15, 2019
Package Status
Not in Commercial Distribution
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 58 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 443 |