Prospect® Ureteral Dilatation Balloon Catheter
by Princeton Medical Scientific Co., Ltd 24 variants
Ref 090700400851-1Model 090400400851-1
Active
CE MDR
Valid until
16 Jan 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberCN26/00000404 | Date16 Jan 2026 | StatusActive |
Certificates
- CN26/00000404 Active
Quality management system EU MDR
- Certifier
- SGS Belgium NV 1639
- Issued
- 16 Jan 2026
- Expires
- 16 Jan 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Sterile Single Use Ureteral Dilatation Balloon Catheter
- Model / Reference
- 090400400851-1, 090700400851-1
- Primary DI / UDI-DI
- 06935456208899
- Basic UDI-DI
- 69354562PLYL09XT
- Direct Marketing DI
- 06935456208899
- EMDN Code
- U030202 Ureteral dilators, with balloon
- Device Class
- Class I
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- CN-MF-000018402
- Authorised representative
- Wellkang Ltd XI-AR-000001836
Other devices from Princeton Medical Scientific Co., Ltd
See all devices from Princeton Medical Scientific 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