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Apex™

FDA UDI

Class II (US FDA UDI)

by Boston Scientific

Identity

Trade Name
Apex™ FDA UDI
Generic Name
Coronary angioplasty balloon catheter, basic FDA UDI
Device Name
PTCA Dilatation Catheter FDA UDI
Model / Reference
H7493895915300 FDA UDI
Description
PTCA Dilatation Catheter FDA UDI

Identifiers

Primary DI / UDI-DI
08714729475637 FDA UDI
PMA Number
P860019 FDA UDI
FDA Product Code
LOX FDA UDI
GMDN Term
Coronary angioplasty balloon catheter, basic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.5100 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: Coronary angioplasty balloon catheter, basic

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

Similar devices

Also classified as Coronary angioplasty balloon catheter, basic.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Boston Scientific

Sources (1)

  • FDA UDI ba8cb57d-fe30-4ad5-ac9b-1813e8d249b9 35 fields · synced Jun 1, 2026