ZENFlow
by Zylox-Tonbridge Medical Technology Co., Ltd. 744 variants
Ref ZW180050010018B
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-06970596425591 06970596425591 | Date21 Oct 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- Withdrawn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
- PTA Balloon Catheter
- Model / reference
- ZW180050010018B
- Primary DI / UDI-DI
- 06970596425591
- Basic UDI-DI
- B-06970596425591
- EMDN code
- C010402020101 PTA balloon dilatation catheters
- Device class
- Class IIa
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Poland
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