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Guide sleeve 3.04.080Q4

by Thommen Medical AG

Guide sleeve 3.04.080Q4 is a Class I device made by Thommen Medical AG, listed in FDA GUDID since 13 Jul 2020 (UDI-DI 07640182640620), 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 Number07640182640620 UDI-DI Date13 Jul 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  • Withdrawn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
Guide sleeve
Generic name
Orthopaedic implantation sleeve, single-use
Model / reference
3.04.080Q4
Primary DI / UDI-DI
07640182640620
FDA product code
NDP
GMDN term
Orthopaedic implantation sleeve, single-use
Device class
Class I
Regulation number
872.3980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Orthopaedic implantation sleeve, single-use

Similar devices in this category

Other devices filed under Orthopaedic implantation sleeve, single-use.

Other devices from Thommen Medical AG

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Properties

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