FDA UDI In Commercial Distribution 🇺🇸 United States

ANAX™ 5.5 SPINAL SYSTEM

DI: 08800015989534 · Model: SFS1009 · 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
08800015989534
Version / Model
SFS1009
Company Name
Innosys Co., Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-10
Public Version
3
Public Version Date
2023-06-19
Public Version Status
Update
Public Device Record Key
7189c0cf-5706-439f-b8ec-68ff5fe1a005

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
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
HXX SCREWDRIVER

GMDN Terms

Code Name
32865 Orthopaedic implant driver

Identifiers

Type ID
Primary 08800015989534