FDA UDI In Commercial Distribution 🇺🇸 United States

ANAX™ 5.5 SPINAL SYSTEM

DI: 08800037511584 · Model: SFA7560 · Innosys Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANAX™ 5.5 SPINAL SYSTEM
Primary DI
08800037511584
Version / Model
SFA7560
Company Name
Innosys Co., Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-10-04
Public Version
2
Public Version Date
2023-06-19
Public Version Status
Update
Public Device Record Key
ee5da077-eadc-4a14-bd44-40f42d6a7e1f

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
Yes
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
NKB Thoracolumbosacral pedicle screw system

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 08800037511584

Premarket Submissions

Submission Number Supplement Number
K132101 000