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Medline OR12L

by Medline Industries, Inc.

Medline OR12L is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 29 Jan 2021 (UDI-DI 10888277634268), 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 Number10888277634268 UDI-DI Date29 Jan 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  • Withdrawn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

Trade name
Medline
Generic name
Suction/irrigation system canister/bottle holder, single-use
Model / Ref / Catalog
OR12L
Primary DI / UDI-DI
10888277634268
FDA product code
KDQ
GMDN term
Suction/irrigation system canister/bottle holder, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code KDQ (BOTTLE, COLLECTION, VACUUM).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)