AuroSlim SK22215
by Aurolab
AuroSlim SK22215 is a Class I device made by Aurolab, listed in FDA GUDID since 15 Jun 2023 (UDI-DI 10803878053201), not in commercial distribution (GUDID) 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 | Number10803878053201 | Date15 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 10803878053201
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- AuroSlim
- Generic name
- Ophthalmic knife, single-use
- Model / reference
- SK22215
- Primary DI / UDI-DI
- 10803878053201
- FDA product code
- HNN
- GMDN term
- Ophthalmic knife, single-use
- Device class
- Class I
- Regulation number
- 886.4350
- GUDID distribution status
- Not in Commercial Distribution
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- PRISMA DISPOSABLE MVR/STILETTO BLADE by Advanced Surgical Products, Inc.