OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE - Biomet Uk Ltd

Duns Number:219322575

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More Product Details

Catalog Number

32-420726

Brand Name

OXFORD UNICOMPARTMENTAL KNEE PHASE 3FEMORAL INSTRUMENT CASE

Version/Model Number

32-420726

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

-

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

FSM

Product Code Name

TRAY, SURGICAL, INSTRUMENT

Device Record Status

Public Device Record Key

aa9a5a21-5ba8-4462-be01-bf102fd11f9e

Public Version Date

September 16, 2022

Public Version Number

5

DI Record Publish Date

May 23, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIOMET UK LTD" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 796
2 A medical device with a moderate to high risk that requires special controls. 137
3 A medical device with high risk that requires premarket approval 261