FDA UDI In Commercial Distribution 🇺🇸 United States

CannuLink

DI: 00846832035748 · Model: IFS-040-16L · TORNIER, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CannuLink
Primary DI
00846832035748
Version / Model
IFS-040-16L
Catalog Number
IFS-040-16L
Company Name
TORNIER, INC.
Labeler DUNS
968990812
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-09
Public Version
1
Public Version Date
2022-08-17
Public Version Status
New
Public Device Record Key
ff3a9355-945f-4d91-ad35-3e83b5a8c852

Device Description

GUIDE WIRE

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
Yes
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
FZX Guide, surgical, instrument

GMDN Terms

Code Name
47900 Orthopaedic implant calibration pin

Identifiers

Type ID
Primary 00846832035748

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 1.6 Millimeter
Device Size Text, specify Size LONG