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Wallstent™ Biliary

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
WALLSTENT™ BILIARY FDA UDI
Generic Name
Bare-metal biliary stent FDA UDI
Device Name
Endoscopic Biliary Endoprosthesis FDA UDI
Model / Reference
H965430100 FDA UDI
Description
Endoscopic Biliary Endoprosthesis FDA UDI

Identifiers

Primary DI / UDI-DI
08714729204633 FDA UDI
FDA Product Code
MUM FDA UDI
FGE FDA UDI
MQR FDA UDI
JCT FDA UDI
ESW FDA UDI
GMDN Term
Bare-metal biliary stent FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.3610 FDA UDI
876.5010 FDA UDI
878.3720 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: Bare-metal biliary stent

Wallstent™ Biliary by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal biliary stent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI af15b42b-c695-401a-8331-108ac8fa82c0 34 fields · synced May 30, 2026