PULSAVAC® - ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.

Duns Number:137354267

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More Product Details

Catalog Number

00-5150-475-01

Brand Name

PULSAVAC®

Version/Model Number

00-5150-475-01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FQH

Product Code Name

LAVAGE, JET

Device Record Status

Public Device Record Key

901b204c-5f72-414e-a9f0-9d867ba3f834

Public Version Date

August 23, 2022

Public Version Number

5

DI Record Publish Date

June 01, 2016

Additional Identifiers

Package DI Number

00889024380042

Quantity per Package

10

Contains DI Package

00889024375161

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1447
2 A medical device with a moderate to high risk that requires special controls. 96