Priflex® Trachealkanüle, drahtverstärkt-flexibel, gesiebt, Gr.9
by Primed Halberstadt Medizintechnik GmbH
Ref 200811, 200821Model Priflex Kanülen
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 | Number42502032PRI0695C | Date5 May 2025 | 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- Withdrawn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
- Trade Name
- Priflex® Trachealkanüle, drahtverstärkt-flexibel, gesiebt, Gr.9Priflex® Trachealkanüle, drahtverstärkt-flexibel mit Cuff, gesiebt, Gr.9
- Model / Reference
- Priflex Kanülen, 200811, 200821
- Primary DI / UDI-DI
- 04250203217477, 04250203221122
- Basic UDI-DI
- 42502032PRI0695C
- EMDN Code
- R0105010202, R0105020202
- Device Class
- Class IIb
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000004967
Other devices from Primed Halberstadt Medizintechnik GmbH
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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