Skip to content

Medline DYNDT1091

by Medline Industries, Inc.

Medline DYNDT1091 is an indwelling urethral catheterization kit (FDA Class II; FDA product code OHR, Catheter care tray) made by Medline Industries, Inc., listed in FDA GUDID since 14 Oct 2016 (UDI-DI 10884389868485), 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 Number10884389868485 UDI-DI Date14 Oct 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  • Withdrawn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
Medline
Generic name
Indwelling urethral catheterization kit, adult
Model / Ref / Catalog
DYNDT1091
Primary DI / UDI-DI
10884389868485
FDA product code
OHR
GMDN term
Indwelling urethral catheterization kit, adult
Device class
Class II
Regulation number
876.5130
GUDID distribution status
In Commercial Distribution

Related devices

Category: Indwelling urethral catheterization kit, adult

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (8, all answered No)