FDA UDI Not in Commercial Distribution 🇺🇸 United States

DURAFORM

DI: 10886704079477 · Model: 80-1477US · Cerenovus, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DURAFORM
Primary DI
10886704079477
Version / Model
80-1477US
Catalog Number
801477US
Company Name
Cerenovus, Inc.
Labeler DUNS
607846297
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-22
Public Version
7
Public Version Date
2023-09-15
Public Version Status
Update
Public Device Record Key
7d508397-585a-4a3a-a91f-9c649c9d43f5
Distribution End Date
2022-09-01

Device Description

DURAFORM Dural Graft Implant 3 Inches x 3 Inches (7.62cm x 7.62cm)

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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
Primary 10886704079477

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K152481 000