i-ED COIL 392-0615
by Kaneka Corp. Japan GUDID
Product code HCG
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04540778177086 | Date10 Dec 2025 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- i-ED COIL
- Generic Name
- Non-neurovascular embolization coil
- Model / Ref / Catalog
- 392-0615
- Primary DI / UDI-DI
- 04540778177086
- 510(k) Number
- FDA Product Code
- HCG, KRD
- GMDN Term
- Non-neurovascular embolization coil
- Device Class
- Class II
- Regulation Number
- 882.5950, 870.3300
- Commercial Distribution
- In Commercial Distribution
- MRI Safety
- MR Conditional
Other devices from Kaneka Corp.
Properties & raw data
Show properties, registry sources and raw records
Other properties (8)
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No
Sources (1)
- FDA UDI 1d5ea95d-248b-4182-a81a-193e1a15594c