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Oz 1705604

by Berchtold Holding GmbH

Oz 1705604 is a Class I device made by Berchtold Holding GmbH, listed in FDA GUDID since 25 May 2021 (UDI-DI 07613327170467), 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 Number07613327170467 UDI-DI Date25 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  • Withdrawn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
Urological operating table top
Model / Ref / Catalog
OZ 1705604
Description
TUR position module, Operon D 750-D 850, EU. Keep Dry.
Primary DI / UDI-DI
07613327170467
FDA product code
CCX
GMDN term
Urological operating table top
Device class
Class I
Regulation number
868.6820
GUDID distribution status
In Commercial Distribution

Related devices

Category: Urological operating table top

Other devices from Berchtold Holding GmbH

See all devices from Berchtold Holding GmbH →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)