Ritter 9A337001-814
Ritter 9A337001-814 is a Class I device made by Midmark Corporation, listed in FDA GUDID since 7 May 2020 (UDI-DI 00841709111341), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841709111341 | Date7 May 2020 | StatusListed |
Official records
- AccessGUDID record 00841709111341
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Ritter
- Generic name
- Footrest
- Model / Ref / Catalog
- 9A337001-814
- Primary DI / UDI-DI
- 00841709111341
- FDA product code
- GBB
- GMDN term
- Footrest
- Device class
- Class I
- Regulation number
- 878.4960
- GUDID distribution status
- In Commercial Distribution
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