FDA UDI In Commercial Distribution 🇺🇸 United States

Lumbar Plate

DI: M719GLPF60220 · Model: 1 · Genesys Orthopedics Systems LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Lumbar Plate
Primary DI
M719GLPF60220
Version / Model
1
Catalog Number
GLPF6022
Company Name
Genesys Orthopedics Systems LLC
Labeler DUNS
017921066
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-11-08
Public Version
5
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
b7b4a233-4318-4e81-8fd9-945eeb0187ee

Device Description

22mm Lumbar Plate Fixed Rescue Screw

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M719GLPF60220

Customer Contacts

Phone
5123817070

Device Sizes

Type Value Unit Text
Length 22 Millimeter