← Back to catalogue

Express® SD Renal/Biliary

FDA UDI

Class III (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Express® SD Renal/Biliary FDA UDI
Generic Name
Peripheral artery stent, bare-metal FDA UDI
Device Name
Premounted Stent System FDA UDI
Model / Reference
H74937911715150 FDA UDI
Description
Premounted Stent System FDA UDI

Identifiers

Catalog Number
H74937911715150 FDA UDI
Primary DI / UDI-DI
08714729390435 FDA UDI
FDA Product Code
NIN FDA UDI
FGE FDA UDI
GMDN Term
Peripheral artery stent, bare-metal 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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Peripheral angioplasty balloon catheter, basicPeripheral artery stent, bare-metal

Express® SD Renal/Biliary 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 5b696f67-0d5a-403d-b97a-2b50bce7f113 35 fields · synced May 31, 2026