Powerflex

FDA UDI

Class II (US FDA UDI)

by Cordis US Corp.

Identity

Trade Name: POWERFLEX FDA UDI
Generic Name: Peripheral angioplasty balloon catheter, basic FDA UDI
Device Name: POWERFLEX P3 F5 9X2 135 FDA UDI
Model / Reference: 4209020X FDA UDI
Description: POWERFLEX P3 F5 9X2 135 FDA UDI

Identifiers

Catalog Number: 4209020X FDA UDI
Primary DI / UDI-DI: 20705032004906 FDA UDI
510(k) Number: K032737 FDA UDI
FDA Product Code: DQY 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Peripheral angioplasty balloon catheter, basic

Powerflex by Cordis US Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peripheral angioplasty balloon catheter, basic.

Minerva PTA Balloon Dilatation Catheter — BrosMed Medical Co., Ltd. · Class IIa
Advocate™ — Merit Medical Systems, Inc. · Class II
Senri — KANEKA Corporation · Class IIa
Jade PTA Balloon Dilatation Catheter — OrbusNeich Medical (ShenZhen) Co., Ltd. · Class II
ZENFluxion — Zylox-Tonbridge Medical Technology Co., Ltd. · Class III
Pacific™ Plus — MEDTRONIC, INC. · Class II
Metacross OTW — KANEKA Corporation · Class IIa
Armada — Abbott Vascular · Class II

Cleared under the same submission

K032737 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Cordis US Corp.

Sources (1)

FDA UDI f8b23b80-6777-4679-b1e8-539c91532374 36 fields · synced Jun 6, 2026