FDA UDI In Commercial Distribution 🇺🇸 United States

Perfix™ Iliac Screw System

DI: 08800015931540 · Model: SL0221 · Innosys Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Perfix™ Iliac Screw System
Primary DI
08800015931540
Version / Model
SL0221
Company Name
Innosys Co., Ltd.
Labeler DUNS
688811082
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-24
Public Version
5
Public Version Date
2023-06-19
Public Version Status
Update
Public Device Record Key
5c301087-df9f-4edf-a749-7f2c389c7b2e

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
MNH Orthosis, spondylolisthesis spinal fixation

GMDN Terms

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

Identifiers

Type ID
Primary 08800015931540

Premarket Submissions

Submission Number Supplement Number
K132218 000

Storage Conditions

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