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WALLSTENT™ RP Endoprosthesis

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name
WALLSTENT™ RP Endoprosthesis FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
Self-Expanding Stent FDA UDI
Model / Reference
M001711320 FDA UDI
Description
Self-Expanding Stent FDA UDI

Identifiers

Primary DI / UDI-DI
08714729406433 FDA UDI
FDA Product Code
MAF FDA UDI
JCT FDA UDI
FGE FDA UDI
GMDN Term
Peripheral artery stent, bare-metal FDA UDI

Classification

Device Class
Class III FDA UDI
Regulation Number
878.3720 FDA UDI
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
MRI Safety
MR Conditional FDA UDI

Category: Peripheral artery stent, bare-metal

WALLSTENT™ RP Endoprosthesis by Boston Scientific — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral artery stent, bare-metal.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 2543e5a5-844e-4c66-93f1-4355ad590a68 34 fields · synced May 31, 2026