Instrumentarium s.50.173
by Société Chirurgicale Instrumentarium Inc
Instrumentarium s.50.173 is a Class I device made by Société Chirurgicale Instrumentarium Inc, listed in FDA GUDID since 11 Aug 2021 (UDI-DI 00810055472079), 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 | Number00810055472079 | Date11 Aug 2021 | StatusListed |
Official records
- AccessGUDID record 00810055472079
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Instrumentarium
- Generic name
- Paranasal sinus irrigation/aspiration cannula
- Model / reference
- s.50.173
- Primary DI / UDI-DI
- 00810055472079
- FDA product code
- KAM
- GMDN term
- Paranasal sinus irrigation/aspiration cannula
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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