FDA UDI In Commercial Distribution 🇺🇸 United States

CorticaLINK MI

DI: 00817329023265 · Model: 80-4716 · LINKSPINE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CorticaLINK MI
Primary DI
00817329023265
Version / Model
80-4716
Catalog Number
80-4716
Company Name
LINKSPINE, INC.
Labeler DUNS
067584601
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-24
Public Version
4
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
b9ae7a24-6269-4b80-b149-9321bee170f2

Device Description

Guidewire, 500mm, Blunt

Device Characteristics

Single Use
No
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
Yes
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
GDF Guide, Needle, Surgical

GMDN Terms

Code Name
62729 Orthopaedic guidewire, single-use

Identifiers

Type ID
Primary 00817329023265

Customer Contacts