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Medicon 58.47.10

by Medicon eG. Chirurgiemechaniker-Genossenschaft

Medicon 58.47.10 is a Class II device made by Medicon eG. Chirurgiemechaniker-Genossenschaft, listed in FDA GUDID since 31 May 2017 (UDI-DI 04046826091309), 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 Number04046826091309 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  • Withdrawn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
Aneurysm clip
Model / Ref / Catalog
58.47.10
Primary DI / UDI-DI
04046826091309
FDA product code
HCH
GMDN term
Aneurysm clip
Device class
Class II
Regulation number
882.5200
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
MRI safety
MR Unsafe

Related devices

Category: Aneurysm clip

Other devices from Medicon eG. Chirurgiemechaniker-Genossenschaft

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Properties

  • Sterilise before use
  • Single use
  • Implantable
  • Prescription use
  • Serial number
Other properties (10, all answered No)