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Medicon 09.82.28

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Medicon 09.82.28 is a Class II device made by Medicon eG. Chirurgiemechaniker-Genossenschaft, listed in FDA GUDID since 31 May 2017 (UDI-DI 04046826013165), 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 Number04046826013165 UDI-DI Date31 May 2017ListedStatusListed 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  • Withdrawn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
Medicon
Generic name
Suction cannula, reusable
Model / Ref / Catalog
09.82.28
Primary DI / UDI-DI
04046826013165
FDA product code
JOL
GMDN term
Suction cannula, reusable
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Suction cannula, reusable

Similar devices in this category

Other devices filed under Suction cannula, reusable.

Other devices from Medicon eG. Chirurgiemechaniker-Genossenschaft

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Properties

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