FDA UDI In Commercial Distribution 🇺🇸 United States

Guidewire Kit

DI: 10855068008119 · Model: CGK-001 · Curvafix Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Guidewire Kit
Primary DI
10855068008119
Version / Model
CGK-001
Catalog Number
CGK-001
Company Name
Curvafix Inc
Labeler DUNS
039779098
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-08-11
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
8fc88f7d-4247-4ef1-82e6-1170c25af894

Device Description

A single use kit, composed of a sterile packaged Steerable Guide, Driving Guidewire and Exchange Tube, that is used during a surgical procedure for the placement of the CurvaFix IM Implant.

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
62729 Orthopaedic guidewire, single-use

Identifiers

Type ID
Primary 10855068008119

Customer Contacts

Phone
425-276-8800