FDA UDI In Commercial Distribution 🇺🇸 United States

Versatex

DI: 10884521532298 · Model: VTX5050M · SOFRADIM PRODUCTION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Versatex
Primary DI
10884521532298
Version / Model
VTX5050M
Company Name
SOFRADIM PRODUCTION
Labeler DUNS
576342646
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-04-15
Public Version
14
Public Version Date
2023-10-31
Public Version Status
Update
Public Device Record Key
4e03d1cc-7902-4cdb-a3d6-47c356aae257

Device Description

Monofilament Mesh, Macroporous Polyester

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
No
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 10884521532298

Customer Contacts

Device Sizes

Type Value Unit Text
Length 50 Centimeter
Width 50 Centimeter