FDA UDI In Commercial Distribution 🇺🇸 United States

Axis Spine Technologies ALIF System Instrument

DI: 05056619800413 · Model: 2984 00 310 · AXIS SPINE TECHNOLOGIES LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Axis Spine Technologies ALIF System Instrument
Primary DI
05056619800413
Version / Model
2984 00 310
Catalog Number
2984 00 310
Company Name
AXIS SPINE TECHNOLOGIES LTD
Labeler DUNS
221947288
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-17
Public Version
1
Public Version Date
2023-05-25
Public Version Status
New
Public Device Record Key
f04d50cf-628e-42f0-b85b-11254b3a1ad9

Device Description

Sterilisation Case - Inner Layer (2 of 2)

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
No
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 05056619800413

Customer Contacts