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Medicon 52.23.33

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Medicon 52.23.33 is a Class I device made by Medicon eG. Chirurgiemechaniker-Genossenschaft, listed in FDA GUDID since 24 Sep 2020 (UDI-DI 04046826064297), 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 Number04046826064297 UDI-DI Date24 Sep 2020ListedStatusListed 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  • Withdrawn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
Vaginal speculum, reusable
Model / Ref / Catalog
52.23.33
Primary DI / UDI-DI
04046826064297
FDA product code
HDL
GMDN term
Vaginal speculum, reusable
Device class
Class I
Regulation number
884.4520
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Vaginal speculum, 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)