8697400830140
by Tekno Mar Maki̇na İmal.i̇th. İhr. San. Ti̇c. Ltd. Şti̇.
Ref HRF 3000 D125Model HRF 3000 S30
Active
CE MDR CE MDD
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/MDD | Number869740083HPPSTRDEVDK 08697400830140 | Date8 Oct 2026 | StatusActive |
| European Union | CE/MDR | Number869740083HPPSTRDEVDK 08697400830140 | Date8 Oct 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Trade Name
- 8697400830140HRF3000
- Device Name
- 30 L Single-Door Hydrogen Peroxide (H2O2) Plasma Sterilization Device125 L Double-Door Hydrogen Peroxide (H₂O₂) Plasma Sterilization Device
- Model / Reference
- HRF 3000 S30, HRF 3000 D125
- Primary DI / UDI-DI
- 08697400830140
- Basic UDI-DI
- 869740083HPPSTRDEVDK, B-08697400830140
- Direct Marketing DI
- 08697400830140
- EMDN Code
- Z12011309 Plasma sterilisers
- Device Class
- Class IIaClass IIb
- EU market of registration
- Romania
Manufacturer details
- EUDAMED SRN
- TR-MF-000017202
Other devices from Tekno Mar Maki̇na İmal.i̇th. İhr. San. Ti̇c. Ltd. Şti̇.
See all devices from Tekno Mar Maki̇na İmal.i̇th. İhr. San. Ti̇c. Ltd. Şti̇. →
Properties
Other properties (13)
- Sterile: No
- 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