FDA UDI In Commercial Distribution 🇺🇸 United States

Perfix™ Spinal System

DI: 08800015953900 · Model: SN0921 · Innosys Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Perfix™ Spinal System
Primary DI
08800015953900
Version / Model
SN0921
Company Name
Innosys Co., Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-01
Public Version
10
Public Version Date
2023-06-19
Public Version Status
Update
Public Device Record Key
1cf2f22a-52a4-4292-b1fb-d751af2356f4

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
FSM TRAY, SURGICAL, INSTRUMENT

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 08800015953900

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool dry place.