FDA UDI In Commercial Distribution 🇺🇸 United States

ANODYNE Plate System

DI: M72520003048 · Model: 20003-048 · CORELINK LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ANODYNE Plate System
Primary DI
M72520003048
Version / Model
20003-048
Catalog Number
20003-048
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
5
Public Version Date
2025-07-02
Public Version Status
Update
Public Device Record Key
57a5ff7d-a817-4ffc-9657-4d6a57848ba9

Device Description

ANODYNE CERVICAL PLATE - 3 LEVEL, 48MM

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 M72520003048

Customer Contacts

Device Sizes

Type Value Unit Text
Height 48 Millimeter