Rhino Stomper - Large
Rhino Stomper - Large (27327) is a Class I device made by MD Orthopaedics, listed in FDA GUDID since 29 Dec 2023 (UDI-DI 00810060887745), 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 | Number00810060887745 | Date29 Dec 2023 | StatusListed |
Official records
- AccessGUDID record 00810060887745
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Rhino
- Generic name
- Cast boot
- Model / Ref / Catalog
- Rhino Stomper - Large, 27327
- Primary DI / UDI-DI
- 00810060887745
- FDA product code
- IQI
- GMDN term
- Cast boot
- Device class
- Class I
- Regulation number
- 890.3475
- GUDID distribution status
- In Commercial Distribution
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