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Curaplex 12186

by Bound Tree Medical, LLC

Curaplex 12186 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 16 Dec 2016 (UDI-DI 00815277020084), 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 Number00815277020084 UDI-DI Date16 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  • Withdrawn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
Nasogastric feeding tube
Model / Ref / Catalog
12186
Primary DI / UDI-DI
00815277020084
FDA product code
FMF, POQ, KDH
GMDN term
Nasogastric feeding tube
Device class
Class II
Regulation number
880.5860, 880.5440, 876.5980
GUDID distribution status
In Commercial Distribution

Related devices

Category: General-purpose syringe, single-useNasogastric feeding tubeStopcockUmbilical cord tape

Similar devices

Other devices filed under FDA product code FMF (Syringe, piston).

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)