LACTOSORB* 2.0MM SYSTEM TEMPLATE - BIOMET MICROFIXATION, INC

Duns Number:046189866

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More Product Details

Catalog Number

914-2112

Brand Name

LACTOSORB* 2.0MM SYSTEM TEMPLATE

Version/Model Number

914-2112

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

July 27, 2020

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

HWT

Product Code Name

TEMPLATE

Device Record Status

Public Device Record Key

2dfc591b-5ec0-4733-94d3-8043d8614d64

Public Version Date

July 27, 2020

Public Version Number

2

DI Record Publish Date

September 14, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"BIOMET MICROFIXATION, INC" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 1783
2 A medical device with a moderate to high risk that requires special controls. 11874
3 A medical device with high risk that requires premarket approval 34