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Protégé™ GPS™

FDA UDI

Class II (US FDA UDI)

by Ev3, Inc

Identity

Trade Name
Protégé™ GPS™ FDA UDI
Generic Name
Bare-metal biliary stent FDA UDI
Device Name
STENT SERB65-14-60-80 PROTEGE GPS V05 FDA UDI
Model / Reference
SERB65-14-60-80 FDA UDI
Description
STENT SERB65-14-60-80 PROTEGE GPS V05 FDA UDI

Identifiers

Primary DI / UDI-DI
00821684071762 FDA UDI
510(k) Number
K021729 FDA UDI
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

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6.0 French FDA UDI
Length — 60.0 Millimeter FDA UDI

Category: Bare-metal biliary stent

Protégé™ GPS™ by Ev3, Inc — 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
Ev3, Inc

Sources (1)

  • FDA UDI 463dffc7-5d2e-4983-9123-69363bc53bb3 37 fields · synced May 31, 2026