Identity
- Trade Name
- Protégé EverFlex™ FDA UDI
- Generic Name
- Bare-metal biliary stent FDA UDI
- Device Name
- STENT PRB35-05-020-080 PROTEGE EF V08 FDA UDI
- Model / Reference
- PRB35-05-020-080 FDA UDI
- Description
- STENT PRB35-05-020-080 PROTEGE EF V08 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00821684068496 FDA UDI
- 510(k) Number
- K072301 FDA UDI
- FDA Product Code
- NIP FDA UDIFGE FDA UDI
- GMDN Term
- Bare-metal biliary stent FDA UDI
Classification
- Device Class
- Class III 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
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Length — 20.0 Millimeter FDA UDICatheter Gauge — 6.0 French FDA UDI
Category: Bare-metal biliary stent
Protégé EverFlex™ by Ev3, Inc — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Bare-metal biliary stent.
- ALIMAXX-B® — Merit Medical Systems, Inc. · Class II
- PALMAZ GENESIS Transhepatic Biliary Stent on OPTA PRO .035" Delivery System — Cordis US Corp. · Class II
- LifeStar® Biliary Stent — Bard Peripheral Vascular · Class II
- SMART FLEX — Cordis US Corp. · Class II
- BONASTENT® Biliary — Sewoon Medical Co., Ltd. · Class II
- Palmaz BLUE Transhepatic Biliary Stent on SLALOM .018 System — Cordis US Corp. · Class II
- Valeo® Balloon Expandable Biliary Stent — Bard Peripheral Vascular · Class II
- E·Luminexx® Biliary Stent — Bard Peripheral Vascular · Class II
Cleared under the same submission
K072301 also covers:
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
- Protege EverFlex — Covidien LP
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Ev3, Inc
Sources (1)
- FDA UDI 35edfde5-4e12-49fc-9fb6-7da3ac35f8e8 37 fields · synced Jun 6, 2026