DuraGen Plus™ Dural Regeneration Matrix - DuraGen Plus™ Dural Regeneration Matrix is an - Integra Lifesciences Corporation

Duns Number:083171244

Device Description: DuraGen Plus™ Dural Regeneration Matrix is an absorbable implant for repair of dural defec DuraGen Plus™ Dural Regeneration Matrix is an absorbable implant for repair of dural defects. DuraGen Plus™ is an easy to handle, soft, white, pliable, nonfriable, porous collagen matrix. DuraGen Plus™ is supplied sterile, nonpyrogenic, for single use in double peel packages in a variety of sizes.

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More Product Details

Catalog Number

DP5013

Brand Name

DuraGen Plus™ Dural Regeneration Matrix

Version/Model Number

DP5013

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

K032693,K032693

Product Code Details

Product Code

GXQ

Product Code Name

DURA SUBSTITUTE

Device Record Status

Public Device Record Key

57b146a8-54e8-4107-b056-2410d5c4362a

Public Version Date

October 04, 2022

Public Version Number

6

DI Record Publish Date

September 22, 2015

Additional Identifiers

Package DI Number

30381780070928

Quantity per Package

5

Contains DI Package

10381780070924

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX

"INTEGRA LIFESCIENCES CORPORATION" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 14
2 A medical device with a moderate to high risk that requires special controls. 75
3 A medical device with high risk that requires premarket approval 17
U Unclassified 32