Sklar 96-2598M
Sklar 96-2598M is a Class I device made by Sklar Corporation, listed in FDA GUDID since 16 May 2019 (UDI-DI 50649111400924), registry data as of 23 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 | Number50649111400924 | Date16 May 2019 | StatusListed |
Official records
- AccessGUDID record 50649111400924
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sklar
- Generic name
- Surgical soft-tissue manipulation forceps, scissors-like, single-use
- Model / reference
- 96-2598M
- Primary DI / UDI-DI
- 50649111400924
- FDA product code
- LRW
- GMDN term
- Surgical soft-tissue manipulation forceps, scissors-like, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
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