Kerecis® Omega3 MariGen® Shield - Bilayer wound management medical device product - KERECIS hf.

Duns Number:365732410

Device Description: Bilayer wound management medical device product made from fish skin and silicone. Kerecis®

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More Product Details

Catalog Number

50215I52B0D

Brand Name

Kerecis® Omega3 MariGen® Shield

Version/Model Number

30 mm Circular

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"

Yes

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

K213231,K213231

Product Code Details

Product Code

KGN

Product Code Name

Dressing, Wound, Collagen

Device Record Status

Public Device Record Key

d758b2fc-35dc-4f98-8526-ef6c01225cf3

Public Version Date

August 30, 2022

Public Version Number

1

DI Record Publish Date

August 22, 2022

Additional Identifiers

Package DI Number

05694310963787

Quantity per Package

10

Contains DI Package

05694310963770

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box

"KERECIS HF." Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 16
U Unclassified 49