Kawana Ns
by Pentamaster MediQ Sdn. Bhd. 34 variants
Ref 805.K2419.NF.KOIModel KAWANA
Active
CE MDR
Valid until
7 Aug 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number955101489KAWANAF9 09551014891180 | Date15 Apr 2026 | StatusActive |
Certificates
- 2024-MDR/QS-051/A Active
Quality management system EU MDR
- Certifier
- 3EC International a.s. 2265
- Issued
- 5 Jan 2026
- Expires
- 7 Aug 2029
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Peripheral IV Catheter
- Model / Reference
- KAWANA, 805.K2419.NF.KOI
- Primary DI / UDI-DI
- 09551014891180
- Basic UDI-DI
- 955101489KAWANAF9
- Direct Marketing DI
- 09551014891180
- EMDN Code
- C0101010101 Peripheral i.v. catheters, w/o safety systems, with injection valves
- Device Class
- Class IIb
- EU market of registration
- Slovakia
Manufacturer details
- EUDAMED SRN
- MY-MF-000049132
- Authorised representative
- Europecert UG (haftungsbeschränkt) DE-AR-000004974
Other devices from Pentamaster MediQ Sdn. Bhd.
Properties
Other properties (11)
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Measuring Function: No
- Incorporates Medicinal Product: No