Zimmer ZFX Component - ZIMMER DENTAL INC.

Duns Number:103167086

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More Product Details

Catalog Number

-

Brand Name

Zimmer ZFX Component

Version/Model Number

INLAYTI

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

EJH

Product Code Name

ALLOY, METAL, BASE

Device Record Status

Public Device Record Key

6ecb0c83-a7f3-4a5e-b3ec-e929001e6609

Public Version Date

March 10, 2022

Public Version Number

5

DI Record Publish Date

October 23, 2015

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"ZIMMER DENTAL INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 312
2 A medical device with a moderate to high risk that requires special controls. 724