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Medline ART1110A

by Medline Industries, Inc.

Medline ART1110A is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 7 Mar 2022 (UDI-DI 10653160351108), 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 Number10653160351108 UDI-DI Date7 Mar 2022ListedStatusListed 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  • Withdrawn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
Arterial blood sampling kit
Model / Ref / Catalog
ART1110A
Primary DI / UDI-DI
10653160351108
FDA product code
CBT
GMDN term
Arterial blood sampling kit
Device class
Class I
Regulation number
868.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Arterial blood sampling kit

Similar devices

Other devices filed under FDA product code CBT (Arterial blood sampling kit).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

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