Duns Number:315018218
Device Description: BRAUN Uterine Depressor, 10 5/8", (270 mm), diam. 24 mm, 28 mm, double ended, non-sterile, BRAUN Uterine Depressor, 10 5/8", (270 mm), diam. 24 mm, 28 mm, double ended, non-sterile, reusable
Catalog Number
EO030R
Brand Name
AESCULAP
Version/Model Number
EO030R
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
KOH
Product Code Name
INSTRUMENT, MANUAL, GENERAL OBSTETRIC-GYNECOLOGIC
Public Device Record Key
bedb4911-1d29-4a5c-a406-d74f206c9160
Public Version Date
April 06, 2021
Public Version Number
3
DI Record Publish Date
April 21, 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 |