FDA UDI In Commercial Distribution 🇺🇸 United States

Hexanium® ACIF

DI: 03663136000107 · Model: AC2-A011-L11C · SPINEVISION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Hexanium® ACIF
Primary DI
03663136000107
Version / Model
AC2-A011-L11C
Company Name
SPINEVISION
Labeler DUNS
390377518
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-09
Public Version
1
Public Version Date
2020-11-17
Public Version Status
New
Public Device Record Key
a69bcde7-6ba0-486b-ae8b-ce3f08823a13

Device Description

Convex Ti Cervical Cage Trial

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
44788 Spinal implant trial

Identifiers

Type ID
Primary 03663136000107

Customer Contacts

Phone
+33153332525

Device Sizes

Type Value Unit Text
Height 11 Millimeter
Height 12 Millimeter