Sklar® 98-4150
Sklar® 98-4150 is a Class I device made by Sklar Corporation, listed in FDA GUDID since 3 Aug 2018 (UDI-DI 10649111312694), 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 | Number10649111312694 | Date3 Aug 2018 | StatusListed |
Official records
- AccessGUDID record 10649111312694
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Sklar®
- Generic name
- Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
- Model / reference
- 98-4150
- Primary DI / UDI-DI
- 10649111312694
- FDA product code
- LRW
- GMDN term
- Ophthalmic soft-tissue manipulation forceps, probe-like, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices in this category
Other devices filed under Ophthalmic soft-tissue manipulation forceps, probe-like, single-use.
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