Catalog Number

-

Brand Name

Biogel® M

Version/Model Number

30570

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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)

Yes

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KGO

Product Code Name

Surgeon's gloves

Public Device Record Key

6c5a3f01-4bfd-425c-840d-171741ced394

Public Version Date

October 31, 2022

Public Version Number

1

DI Record Publish Date

October 21, 2022

Package DI Number

05060097931835

Quantity per Package

4

Contains DI Package

05060097931750

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE