FDA UDI In Commercial Distribution 🇺🇸 United States

GORE SYNECOR Preperitoneal Biomaterial

DI: 00733132653713 · Model: GKWR4050 · W. L. Gore & Associates, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
GORE SYNECOR Preperitoneal Biomaterial
Primary DI
00733132653713
Version / Model
GKWR4050
Catalog Number
GKWR4050
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
2022-11-08
Public Version
1
Public Version Date
2022-11-16
Public Version Status
New
Public Device Record Key
1966a2da-bef7-461f-a6d1-ba08e87ac958

Device Description

GORE SYNECOR PREPERITONEAL 40cmX50cmRectangle 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
Yes
Has Lot/Batch Number
No
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 00733132653713

Customer Contacts

Phone
800-528-8763

Premarket Submissions

Submission Number Supplement Number
K163576 000

Device Sizes

Type Value Unit Text
Width 40 Centimeter
Length 50 Centimeter