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Covidien AG

FDA UDI

Class II (US FDA UDI)

by Degania Silicone Ltd

Identity

Trade Name
Covidien AG FDA UDI
Generic Name
Temperature-monitoring indwelling urethral drainage catheter FDA UDI
Device Name
TSC 14Fr Blue Tip F400(+/-0.1) Sterile FDA UDI
Model / Reference
90056T FDA UDI
Description
TSC 14Fr Blue Tip F400(+/-0.1) Sterile FDA UDI

Identifiers

Primary DI / UDI-DI
30884522000066 FDA UDI
FDA Product Code
EZL FDA UDI
GMDN Term
Temperature-monitoring indwelling urethral drainage catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5130 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI
MRI Safety
MR Safe FDA UDI

Category: Temperature-monitoring indwelling urethral drainage catheter

Covidien AG by Degania Silicone Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temperature-monitoring indwelling urethral drainage catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Degania Silicone Ltd

Sources (1)

  • FDA UDI cc9633ff-fde0-4ca4-9f56-392638824e95 33 fields · synced Jun 1, 2026