FDA UDI In Commercial Distribution 🇺🇸 United States

GORE DUALMESH Biomaterial

DI: 00733132601059 · Model: 1DLMC202 · W. L. Gore & Associates, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
GORE DUALMESH Biomaterial
Primary DI
00733132601059
Version / Model
1DLMC202
Catalog Number
1DLMC202
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
2016-03-07
Public Version
9
Public Version Date
2023-08-29
Public Version Status
Update
Public Device Record Key
4a9c5337-b699-45d8-9942-4181e9272271

Device Description

GORE DUALMESH BIOMATERIAL 18.0cmX24.0cmX2.0mm

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
60300 Extra-gynaecological surgical mesh, synthetic polymer, non-bioabsorbable

Identifiers

Type ID
Primary 00733132601059

Customer Contacts

Phone
8005288763

Premarket Submissions

Submission Number Supplement Number
K992189 000

Device Sizes

Type Value Unit Text
Height 2 Millimeter
Width 18 Centimeter
Length 24 Centimeter