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Medline HCS4483T

by Medline Industries, Inc.

Medline HCS4483T is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 9 Jun 2021 (UDI-DI 10193489021189), 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 Number10193489021189 UDI-DI Date9 Jun 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  • Withdrawn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
Nebulizing system delivery set, single-use
Model / Ref / Catalog
HCS4483T
Primary DI / UDI-DI
10193489021189
FDA product code
CAI
GMDN term
Nebulizing system delivery set, single-use
Device class
Class I
Regulation number
868.5240
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CAI (Circuit, breathing (w connector, adaptor, y piece)).

Other devices from Medline Industries, Inc.

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Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)