FDA UDI In Commercial Distribution 🇺🇸 United States

Hexanium® TLIF

DI: 03663136001302 · Model: TL3-A024 · SPINEVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hexanium® TLIF
Primary DI
03663136001302
Version / Model
TL3-A024
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-19
Public Version
1
Public Version Date
2021-03-29
Public Version Status
New
Public Device Record Key
a8ab45ac-3675-4874-b84f-f2db7bb95d52

Device Description

Ti Straight TLIF Cage Graft Compactor

Device Characteristics

Single Use
No
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
44054 Orthopaedic surgical procedure kit, non-medicated, reusable

Identifiers

Type ID
Primary 03663136001302

Customer Contacts

Phone
+33153332525