Single Use Professional S434
Single Use Professional S434 is a Class II device made by Eakin Surgical Limited, listed in FDA GUDID since 9 Aug 2016 (UDI-DI 05055299106037), 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 | Number05055299106037 | Date9 Aug 2016 | StatusListed |
Official records
- AccessGUDID record 05055299106037
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Single Use Professional
- Generic name
- Surgical irrigation/aspiration cannula, non-illuminating, single-use
- Model / Ref / Catalog
- S434
- Primary DI / UDI-DI
- 05055299106037
- FDA product code
- GCX
- GMDN term
- Surgical irrigation/aspiration cannula, non-illuminating, single-use
- Device class
- Class II
- Regulation number
- 880.6740
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 7 CentimeterNeedle Gauge — 18 Gauge
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