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Covidien

FDA UDI

Class II (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Covidien FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
True content to be populated as part of rebranding FDA UDI
Model / Reference
8884715122E FDA UDI
Description
True content to be populated as part of rebranding FDA UDI

Identifiers

Catalog Number
8884715122E FDA UDI
Primary DI / UDI-DI
10884521661622 FDA UDI
FDA Product Code
KNT FDA UDI
PIF FDA UDI
GMDN Term
Gastrostomy tube FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Gastrostomy tube

Covidien by Cardinalhealth — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrostomy tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI aba08c11-264b-4095-9906-08c56c2246ab 35 fields · synced Jun 8, 2026