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Curaplex 8600-01172

by Bound Tree Medical, LLC

Curaplex 8600-01172 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 14 Dec 2016 (UDI-DI 00815277028028), 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 Number00815277028028 UDI-DI Date14 Dec 2016ListedStatusListed 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  • Withdrawn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
First aid kit, non-medicated, reusable
Model / reference
8600-01172
Primary DI / UDI-DI
00815277028028
FDA product code
CFW
GMDN term
First aid kit, non-medicated, reusable
Device class
Class II
Regulation number
862.1345
GUDID distribution status
In Commercial Distribution

Related devices

Category: First aid kit, non-medicated, reusable

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
Other properties (10, all answered No)