FDA UDI In Commercial Distribution 🇺🇸 United States

ANODYNE Plate System

DI: M7252024518 · Model: 20245-18 · CORELINK LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ANODYNE Plate System
Primary DI
M7252024518
Version / Model
20245-18
Catalog Number
20245-18
Company Name
CORELINK LLC
Labeler DUNS
064191453
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-01-21
Public Version
4
Public Version Date
2023-12-04
Public Version Status
Update
Public Device Record Key
27f4de7b-53bb-4ef3-8480-c2da11b1526e

Device Description

ANODYNE CERVICAL SCREW - VARIABLE SELF TAPPING - 4.5MM X 18MM

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
No
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
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary M7252024518

Customer Contacts

Device Sizes

Type Value Unit Text
Length 18 Millimeter
Outer Diameter 4.5 Millimeter