Renegade™ HI-FLO™ Kit M001183000
by Boston Scientific EUDAMEDGUDID
Active
Ref M001183000
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number01915060000000000000326MZ | Date14 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08714729280750 | Date24 Sep 2016 | StatusIn distribution |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 25 Oct 2026.
Specification
- Trade Name
- Renegade™ HI-FLO™ EUDAMEDRenegade™ HI-FLO™ Kit GUDID
- Generic Name
- Vascular microcatheter
- Device Name
- Renegade Hi-Flo
- Model / Reference
- M001183000
- Primary DI / UDI-DI
- 08714729280750
- Basic UDI-DI
- 01915060000000000000326MZ
- FDA Product Code
- KRA
- EMDN Code
- C0104020202 Peripheral embolisation catheters and microcatheters
- GMDN Term
- Vascular microcatheter
- Device Class
- Class IIb EUDAMEDClass II GUDID
- Regulation Number
- 870.1210
- Commercial Distribution
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIb | Class II |
Other devices from Boston Scientific
Properties
Other properties (16)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No