FDA UDI In Commercial Distribution 🇺🇸 United States

DuraGen®

DI: 10381780023548 · Model: ID1105 · Integra Lifesciences Corporation
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
DuraGen®
Primary DI
10381780023548
Version / Model
ID1105
Catalog Number
ID-1105
Company Name
Integra Lifesciences Corporation
Labeler DUNS
083171244
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-22
Public Version
7
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
6316875a-531b-4e13-870f-ceb01ce9c300

Device Description

DuraGen® Dural Graft Matrix 5 PK, 1x1 DOM

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
GXQ DURA SUBSTITUTE

GMDN Terms

Code Name
48155 Dura mater biomatrix implant

Identifiers

Type ID
Package 30381780023542
Primary 10381780023548
Secondary M269ID11051

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K982180 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 1 in x 1 in 2.5 cm x 2.5 cm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store at Room Temperature.