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Curaplex 301-PrO2LTEZ

by Tri-Anim Health Services, Inc.

Curaplex 301-PrO2LTEZ is a Class II device made by Tri-Anim Health Services, Inc., listed in FDA GUDID since 10 Jan 2024 (UDI-DI 00818834028486), 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 Number00818834028486 UDI-DI Date10 Jan 2024ListedStatusListed 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  • Withdrawn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
Capnography oxygen mask
Model / Ref / Catalog
301-PrO2LTEZ
Primary DI / UDI-DI
00818834028486
FDA product code
CCK
GMDN term
Capnography oxygen mask
Device class
Class II
Regulation number
868.1400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Capnography oxygen mask

Similar devices

Other devices filed under FDA product code CCK (ANALYZER, GAS, CARBON-DIOXIDE, GASEOUS-PHASE).

Other devices from Tri-Anim Health Services, Inc.

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

Properties

  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)