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Curaplex 670146-KIT

by Bound Tree Medical, LLC

Curaplex 670146-KIT is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 18 Sep 2017 (UDI-DI 00817617028187), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817617028187 UDI-DI Date18 Sep 2017ListedStatusListed 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  • Withdrawn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
Cardiopulmonary resuscitation mask, single-use
Model / Ref / Catalog
670146-KIT
Primary DI / UDI-DI
00817617028187
FDA product code
CCT
GMDN term
Cardiopulmonary resuscitation mask, single-use
Device class
Class II
Regulation number
868.5170
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiopulmonary resuscitation mask, single-use

Similar devices in this category

Other devices filed under Cardiopulmonary resuscitation mask, single-use.

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

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