HRF3000
by Tekno Mar Maki̇na İmal.i̇th. İhr. San. Ti̇c. Ltd. Şti̇. 5 variants
Ref HRF 3000 STEKModel 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 08697400830171 | Date8 Oct 2026 | StatusActive |
| European Union | CE/MDR | Number869740083HPPSTRDEVDK 08697400830171 | 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- Withdrawn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
- Device Name
- 30 L Single-Door Hydrogen Peroxide (H2O2) Plasma Sterilization DeviceSingle-Door Hydrogen Peroxide (H₂O₂) Plasma Sterilization Device
- Model / Reference
- HRF 3000 S30, HRF 3000 STEK
- Primary DI / UDI-DI
- 08697400830171
- Basic UDI-DI
- 869740083HPPSTRDEVDK, B-08697400830171
- Direct Marketing DI
- 08697400830171
- 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