FDA UDI In Commercial Distribution 🇺🇸 United States

i-ED COIL

DI: 04540778176522 · Model: 390-0206 · KANEKA CORPORATION
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
i-ED COIL
Primary DI
04540778176522
Version / Model
390-0206
Catalog Number
390-0206
Company Name
KANEKA CORPORATION
Labeler DUNS
690535406
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-30
Public Version
4
Public Version Date
2023-09-11
Public Version Status
Update
Public Device Record Key
efca6299-b2e9-4abe-85c2-1fef393480b4

Device Description

The i-ED COIL is used for vascular embolization with a platinum coil at the target lesion in the patient’s blood vessel.

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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
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
HCG Device, Neurovascular Embolization
KRD Device, Vascular, For Promoting Embolization

GMDN Terms

Code Name
60941 Non-neurovascular embolization coil
60940 Neurovascular embolization coil

Identifiers

Type ID
Primary 04540778176522

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Complex (Silky Soft) 10inch 2mm x 6cm
Device Size Text, specify Compatible Microcatheter inner diameter: 0.33 to 0.48 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a clean and cool place avoiding getting wet and direct sunlight, extreme temperature, or high humidity.