Detrowash
by Detro Healthcare Ki̇mya Sanayi̇ Anoni̇m Şi̇rketi̇ 3 variants
Ref DW-5001 DETROWASH ENDOSCOPE WASHING AND DISINF. DEVICEModel DW-5001
Active
CE MDR
Valid until
16 Jun 2031
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number868009710TF01GH 08680097100078 | Date23 Jun 2026 | StatusActive |
Certificates
- 2975-MED-2616801 Active
Quality management system EU MDR
- Certifier
- SZUTEST Konformitätsbewertungsstelle GmbH 2975
- Issued
- 17 Jun 2026
- Expires
- 16 Jun 2031
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Endoscope Washing and Disinfection Device
- Model / Reference
- DW-5001, DW-5001 DETROWASH ENDOSCOPE WASHING AND DISINF. DEVICE
- Primary DI / UDI-DI
- 08680097100078
- Basic UDI-DI
- 868009710TF01GH
- Direct Marketing DI
- 08680097100078
- EMDN Code
- Z12011311 Endoscope washers
- Device Class
- Class IIb
- EU market of registration
- Türkiye
Manufacturer details
- EUDAMED SRN
- TR-MF-000022410
Other devices from Detro Healthcare Ki̇mya Sanayi̇ Anoni̇m Şi̇rketi̇
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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