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Curaplex 14761

by Bound Tree Medical, LLC 3 variants

Curaplex 14761 is a Class II device made by Bound Tree Medical, LLC, listed in FDA GUDID since 14 Dec 2016 (UDI-DI 00815277023214), 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 Number00815277023214 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  • Withdrawn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
Nasogastric feeding tube
Model / reference
14761
Primary DI / UDI-DI
00815277023214
FDA product code
KNT
GMDN term
Nasogastric feeding tube
Device class
Class II
Regulation number
876.5980
GUDID distribution status
In Commercial Distribution
Sterilisation method
Ethylene Oxide
Size
Catheter Gauge — 16 French

Related devices

Category: Nasogastric feeding tube

Similar devices in this category

Other devices filed under Nasogastric feeding tube.

Other devices from Bound Tree Medical, LLC

See all devices from Bound Tree Medical, LLC →

Properties

  • Supplied sterile
  • Sterilise before use
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (8, all answered No)