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Protege GPS

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Protege GPS FDA UDI
Generic Name
Bare-metal biliary stent FDA UDI
Device Name
Self-Expanding Biliary Stent System FDA UDI
Model / Reference
SERB65-12-30-120 FDA UDI
Description
Self-Expanding Biliary Stent System FDA UDI

Identifiers

Primary DI / UDI-DI
00821684031773 FDA UDI
510(k) Number
K050725 FDA UDI
FDA Product Code
FGE FDA UDI
GMDN Term
Bare-metal biliary stent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5010 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

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI
Length — 30 Millimeter FDA UDI
Outer Diameter — 12 Millimeter FDA UDI

Category: Bare-metal biliary stent

Protege GPS by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal biliary stent.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Covidien LP

Sources (1)

  • FDA UDI 92c57cde-8db1-498b-9ce0-710069ffd87c 37 fields · synced May 30, 2026