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Curaplex 301-142U

by Tri-Anim Health Services, Inc.

Curaplex 301-142U is a Class I device made by Tri-Anim Health Services, Inc., listed in FDA GUDID since 15 Oct 2026 (UDI-DI 00818834029087), registry data as of 2 Nov 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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00818834029087 UDI-DI Date15 Oct 2026ListedStatusListed 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  • Withdrawn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
Curaplex
Generic name
Nasal oxygen cannula, basic
Model / Ref / Catalog
301-142U
Primary DI / UDI-DI
00818834029087
FDA product code
CAT
GMDN term
Nasal oxygen cannula, basic
Device class
Class I
Regulation number
868.5340
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CAT (CANNULA, NASAL, OXYGEN).

Other devices from Tri-Anim Health Services, Inc.

See all devices from Tri-Anim Health Services, Inc. →

Properties

  • Single use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)