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Gateway®

FDA UDI

Class Unclassified (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Gateway® FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
PTA Balloon Catheter FDA UDI
Model / Reference
M0032072209150 FDA UDI
Description
PTA Balloon Catheter FDA UDI

Identifiers

Catalog Number
M0032072209150 FDA UDI
Primary DI / UDI-DI
08714729791201 FDA UDI
FDA Product Code
NJE FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Unclassified FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

Category: Peripheral angioplasty balloon catheter, basic

Gateway® by Boston Scientific — Class Unclassified — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI 2c6eec45-dd59-4874-8ae9-79f9c90af347 35 fields · synced May 30, 2026