Disposable Urinary Hydrophilic Guidewire
by MicroPort Urocare (Jiaxing) Co., Ltd. 3 variants
Ref HS-38-150Model HA-32-150,HS-32-150,HA-35-150,HS-35-150,HA-38-150,HS-38-150
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697182106Y0006B6 16941903600564 | Date8 Apr 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Disposable Urinary Hydrophilic Guidewire
- Model / Reference
- HA-32-150, HS-32-150, HA-35-150, HS-35-150, HA-38-150, HS-38-150
- Primary DI / UDI-DI
- 16941903600564
- Basic UDI-DI
- 697182106Y0006B6
- EMDN Code
- U0601 Urological guidewires, hydrophilic
- Device Class
- Class IIa
- EU market of registration
- Italy
Manufacturer details
- EUDAMED SRN
- CN-MF-000002345
- Authorised representative
- MicroPort Medical B.V. NL-AR-000000166
Other devices from MicroPort Urocare (Jiaxing) Co., Ltd.
See all devices from MicroPort Urocare (Jiaxing) Co., Ltd. →
Properties
Other properties (12)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No