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Unimed 25029P

by Unimed Medical Supplies, Inc.

Unimed 25029P is a Class II device made by Unimed Medical Supplies, Inc., listed in FDA GUDID since 23 Aug 2016 (UDI-DI 06945664845885), 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 Number06945664845885 UDI-DI Date23 Aug 2016ListedStatusListed 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  • Withdrawn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
Unimed
Generic name
Rigid optical cystourethroscope
Model / reference
25029P
Primary DI / UDI-DI
06945664845885
FDA product code
DSA
GMDN term
Rigid optical cystourethroscope
Device class
Class II
Regulation number
870.2900
GUDID distribution status
In Commercial Distribution

Related devices

Category: Rigid optical cystourethroscope

Similar devices in this category

Other devices filed under Rigid optical cystourethroscope.

Other devices from Unimed Medical Supplies, Inc.

See all devices from Unimed Medical Supplies, Inc. →

Properties

  • Lot / batch number
Other properties (14, all answered No)