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WALLSTENT® Endoprosthesis

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
WALLSTENT® Endoprosthesis FDA UDI
Generic Name
Trachea prosthesis FDA UDI
Device Name
Self-Expanding Stent FDA UDI
Model / Reference
H965404120 FDA UDI
Description
Self-Expanding Stent FDA UDI

Identifiers

Catalog Number
H965404120 FDA UDI
Primary DI / UDI-DI
08714729204077 FDA UDI
FDA Product Code
JCT FDA UDI
GMDN Term
Trachea prosthesis FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
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: Trachea prosthesisBare-metal tracheal/bronchial stent

WALLSTENT® Endoprosthesis by Boston Scientific — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bare-metal tracheal/bronchial 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 9fb18166-c766-443f-a0be-e3a4b1d3a0fd 35 fields · synced May 30, 2026