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242073

by Medos International Sàrl

242073 is a Class I device made by Medos International Sàrl, listed in FDA GUDID since 20 May 2021 (UDI-DI 10886705031771), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10886705031771 UDI-DI Date20 May 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  • Withdrawn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

Generic name
Arthroscopic obturator
Model / Ref / Catalog
242073
Primary DI / UDI-DI
10886705031771
FDA product code
NBH
GMDN term
Arthroscopic obturator
Device class
Class I
Regulation number
888.1100
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Arthroscopic obturator

Similar devices in this category

Other devices filed under Arthroscopic obturator.

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)