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2cm Peripheral Cutting Balloon®

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
2cm Peripheral Cutting Balloon® FDA UDI
Generic Name
Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name
Microsurgical Dilatation Device FDA UDI
Model / Reference
M001PCB5020500 FDA UDI
Description
Microsurgical Dilatation Device FDA UDI

Identifiers

Primary DI / UDI-DI
08714729813705 FDA UDI
FDA Product Code
PNO FDA UDI
GMDN Term
Peripheral angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 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

2cm Peripheral Cutting Balloon® by Boston Scientific — Class II — 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 e66b6fc5-a83d-46d0-8ff9-48c6792b86f6 34 fields · synced May 31, 2026