FDA UDI In Commercial Distribution 🇺🇸 United States

Medyssey Poseidon OCT Spinal Fixation System

DI: 08809596878138 · Model: LRPP4058 · Medyssey Co., Ltd.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Medyssey Poseidon OCT Spinal Fixation System
Primary DI
08809596878138
Version / Model
LRPP4058
Company Name
Medyssey Co., Ltd.
Labeler DUNS
688211503
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-20
Public Version
1
Public Version Date
2018-05-21
Public Version Status
New
Public Device Record Key
d122de5e-2449-492d-a7a2-3290b29cb8a9

Device Description

Poseidon Reduction Poly-Axial Screw, 4X58mm, 4.0mm rod

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
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
KWP Appliance, Fixation, Spinal Interlaminal
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

Code Name
57806 Vertebral body prosthesis, non-sterile

Identifiers

Type ID
Primary 08809596878138