Zenflow
by Zylox-Tonbridge Medical Technology Co., Ltd. 744 variants
Ref ZWH075070008035BModel ZWH075070010035B
Active
CE MDD
Valid until
No date given
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD | NumberB-06971971811183 06971971811176 | Date8 Nov 2021 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD Active
Specification
- Device name
- HP PTA Balloon Catheter
- Model / reference
- ZWH075070010035B, ZWH075070008035B
- Primary DI / UDI-DI
- 06971971811176
- Basic UDI-DI
- B-06971971811183
- EMDN code
- C010402020101 PTA balloon dilatation catheters
- Device class
- Class IIa
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Czechia
Manufacturer details
- EUDAMED SRN
- CN-MF-000010626
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Zylox-Tonbridge Medical Technology Co., Ltd.
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Properties
Other properties (11)
- Sterilise before use: No
- Implantable: No
- Reusable: No
- Contains latex: No
- Reprocessed single-use device: No
- Incorporates a substance derived from human blood or plasma: No
- Contains human tissues or cells: No
- Contains animal tissues or cells: No
- Administering medicine: No
- Measuring function: No
- Incorporates a medicinal substance: No