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Powerpulse

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
POWERPULSE FDA UDI
Generic Name
Surgical/orthopaedic lavage control unit FDA UDI
Device Name
POWERPULSE LAVAGE HIP/KNEE DISPOSABLE UNIT WITHOUT SUCTION FDA UDI
Model / Reference
71277005 FDA UDI
Description
POWERPULSE LAVAGE HIP/KNEE DISPOSABLE UNIT WITHOUT SUCTION FDA UDI

Identifiers

Catalog Number
71277005 FDA UDI
Primary DI / UDI-DI
03596010421302 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Surgical/orthopaedic lavage control unit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5475 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical/orthopaedic lavage control unit

Powerpulse by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical/orthopaedic lavage control unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 0d6171f9-1f25-4d28-ba2f-1270f6564362 35 fields · synced Jun 8, 2026