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Pulsavac®

FDA UDI

Class II (US FDA UDI)

by Zimmer Orthopaedic Surgical Products

Identity

Trade Name
PULSAVAC® FDA UDI
Generic Name
Disposable surgical irrigation/aspiration system FDA UDI
Device Name
Component Kit (Low Pressure) FDA UDI
Model / Reference
00-5150-920-00 FDA UDI
Description
Component Kit (Low Pressure) FDA UDI

Identifiers

Catalog Number
00-5150-920-00 FDA UDI
Primary DI / UDI-DI
00889024375246 FDA UDI
FDA Product Code
FQH FDA UDI
GMDN Term
Disposable surgical irrigation/aspiration system 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: Disposable surgical irrigation/aspiration system

Pulsavac® by Zimmer Orthopaedic Surgical Products — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Disposable surgical irrigation/aspiration system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8125ade0-64d8-4a8f-bb4d-384b4919201a 35 fields · synced Jun 6, 2026