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73-532-04

by VBM Medizintechnik GmbH

73-532-04 is a Class I device made by VBM Medizintechnik GmbH, listed in FDA GUDID since 18 Sep 2020 (UDI-DI 04250105611595), 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 Number04250105611595 UDI-DI Date18 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  • Withdrawn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

Generic name
Breathing circuit tube holder
Model / reference
73-532-04
Primary DI / UDI-DI
04250105611595
FDA product code
JAY
GMDN term
Breathing circuit tube holder
Device class
Class I
Regulation number
868.5280
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code JAY (Support, Breathing Tube).

Other devices from VBM Medizintechnik GmbH

See all devices from VBM Medizintechnik GmbH →

Properties

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