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Cure Medical

FDA UDI

Class I (US FDA UDI)

by Convatec, Purchasing Department

Identity

Trade Name
CURE MEDICAL FDA UDI
Generic Name
Low-pressure tubing connector, reusable FDA UDI
Device Name
29" Cure Catheter Extension Tube with Connector FDA UDI
Model / Reference
ET1 FDA UDI
Description
29" Cure Catheter Extension Tube with Connector FDA UDI

Identifiers

Primary DI / UDI-DI
00815947020703 FDA UDI
FDA Product Code
NNZ FDA UDI
GMDN Term
Low-pressure tubing connector, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.5250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 74 Centimeter FDA UDI

Category: Low-pressure tubing connector, reusable

Cure Medical by Convatec, Purchasing Department — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Low-pressure tubing connector, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05587c6f-46fd-40f9-bc67-0b526efdcfff 34 fields · synced Jun 6, 2026