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Curaplex 10369

by Bound Tree Medical, LLC

Curaplex 10369 is a Class I device made by Bound Tree Medical, LLC, listed in FDA GUDID since 4 Sep 2017 (UDI-DI 00817617023236), 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 Number00817617023236 UDI-DI Date4 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  • Withdrawn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
Emergency airway clearance suction pump, manual
Model / Ref / Catalog
10369
Primary DI / UDI-DI
00817617023236
FDA product code
BSY
GMDN term
Emergency airway clearance suction pump, manual
Device class
Class I
Regulation number
868.6810
GUDID distribution status
In Commercial Distribution

Related devices

Category: Emergency airway clearance suction pump, manual

Similar devices

Other devices filed under FDA product code BSY (CATHETERS, SUCTION, TRACHEOBRONCHIAL).

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (12, all answered No)