FDA UDI In Commercial Distribution 🇺🇸 United States

Transorb

DI: 10884521809734 · Model: TSB4030 · SOFRADIM PRODUCTION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Transorb
Primary DI
10884521809734
Version / Model
TSB4030
Company Name
SOFRADIM PRODUCTION
Labeler DUNS
576342646
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-03-08
Public Version
2
Public Version Date
2025-08-18
Public Version Status
Update
Public Device Record Key
cbac756f-8e65-4437-ac0f-a07fc02fa236

Device Description

Self-Gripping Resorbable Mesh Monofilament PLLA/TMC Textile and Grips

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
OWT Mesh, surgical, absorbable, abdominal hernia

GMDN Terms

Code Name
44688 Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable

Identifiers

Type ID
Primary 10884521809734

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233661 000

Device Sizes

Type Value Unit Text
Length 40 Centimeter
Height 30 Centimeter