FDA UDI In Commercial Distribution 🇺🇸 United States

GORE SYNECOR Biomaterial

DI: 00733132635382 · Model: GKFV1015 · W. L. Gore & Associates, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GORE SYNECOR Biomaterial
Primary DI
00733132635382
Version / Model
GKFV1015
Catalog Number
GKFV1015
Company Name
W. L. Gore & Associates, Inc.
Labeler DUNS
967358115
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-03-30
Public Version
8
Public Version Date
2023-12-22
Public Version Status
Update
Public Device Record Key
fc847567-fbd2-4c5b-acef-810265b42816

Device Description

GORE SYNECOR INTRAPERITONEAL 10cmX15cm Oval Biomaterial

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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
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
FTL Mesh, Surgical, Polymeric

GMDN Terms

Code Name
44756 Extra-gynaecological surgical mesh, composite-polymer

Identifiers

Type ID
Primary 00733132635382

Customer Contacts

Phone
8005288763

Premarket Submissions

Submission Number Supplement Number
K152609 000

Device Sizes

Type Value Unit Text
Length 15 Centimeter
Width 10 Centimeter