FDA UDI In Commercial Distribution 🇺🇸 United States

FlexBand

DI: 00850003396248 · Model: TW012 · Artelon
Product Codes
5
GMDN Terms
3
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FlexBand
Primary DI
00850003396248
Version / Model
TW012
Catalog Number
TW012
Company Name
Artelon
Labeler DUNS
066284070
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-04-11
Public Version
4
Public Version Date
2025-08-18
Public Version Status
Update
Public Device Record Key
77fd0c2d-8fac-4ad1-98ff-4df00f3129d0

Device Description

TWIST.12

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue
FTL Mesh, Surgical, Polymeric
HTW Bit, Drill
HXX Screwdriver
QWJ Mesh, Surgical, Polymeric, Resorbable, Orthopedics, Reinforcement Of Ligament

GMDN Terms

Code Name
44688 Extra-gynaecological surgical mesh, synthetic polymer, bioabsorbable
45062 Tendon/ligament bone anchor, non-bioabsorbable
58776 Surgical screwdriver, single-use

Identifiers

Type ID
Primary 00850003396248

Customer Contacts