Duns Number:315018218
Device Description: MANNERFELT (MODIF.) Raspatory, curved, 6 1/8", (155 mm), sharp, width: 6 mm, non-sterile, MANNERFELT (MODIF.) Raspatory, curved, 6 1/8", (155 mm), sharp, width: 6 mm, non-sterile, reusable
Catalog Number
FK543R
Brand Name
AESCULAP
Version/Model Number
FK543R
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
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
-
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
-
Product Code
HTR
Product Code Name
RASP
Public Device Record Key
fded875d-a9d7-458f-b1cb-a7a641df5c21
Public Version Date
August 11, 2022
Public Version Number
3
DI Record Publish Date
April 22, 2020
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 11840 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7088 |
| 3 | A medical device with high risk that requires premarket approval | 37 |