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Cure Medical ET1

by Convatec, Purchasing Department

Cure Medical ET1 is a Class I device made by Convatec, Purchasing Department, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 00815947020703), 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 Number00815947020703 UDI-DI Date24 Sep 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  • Withdrawn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
Cure Medical
Generic name
Low-pressure tubing connector, reusable
Model / reference
ET1
Primary DI / UDI-DI
00815947020703
FDA product code
NNZ
GMDN term
Low-pressure tubing connector, reusable
Device class
Class I
Regulation number
876.5250
GUDID distribution status
In Commercial Distribution
Size
Length — 74 Centimeter

Related devices

Category: Low-pressure tubing connector, reusable

Other devices from Convatec, Purchasing Department

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Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)