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Curaplex 301-062213

by Tri-Anim Health Services, Inc.

Curaplex 301-062213 is a Class II device made by Tri-Anim Health Services, Inc., listed in FDA GUDID since 16 Oct 2026 (UDI-DI 00812574027310), 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 Number00812574027310 UDI-DI Date16 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  • Withdrawn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
Atomizer, non-ventilatory
Model / Ref / Catalog
301-062213
Primary DI / UDI-DI
00812574027310
FDA product code
CAF
GMDN term
Atomizer, non-ventilatory
Device class
Class II
Regulation number
868.5630
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code CAF (Nebulizer (direct patient interface)).

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
  • Manufacturing date
Other properties (11, all answered No)