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Instrumentarium s.50.774

by Société Chirurgicale Instrumentarium Inc

Instrumentarium s.50.774 is a Class I device made by Société Chirurgicale Instrumentarium Inc, listed in FDA GUDID since 11 Aug 2021 (UDI-DI 00810055472246), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00810055472246 UDI-DI Date11 Aug 2021ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Instrumentarium
Generic name
Paranasal sinus irrigation/aspiration cannula
Model / reference
s.50.774
Primary DI / UDI-DI
00810055472246
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

Similar devices

Other devices filed under FDA product code KAM (Cannula, Sinus).

Other devices from Société Chirurgicale Instrumentarium Inc

See all devices from Société Chirurgicale Instrumentarium Inc →

Properties

  • Sterilise before use
  • Premarket exempt
Other properties (13, all answered No)