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Ratchet BioniQ
EUDAMEDClass I (EU MDR)
Ref 2408.00Model Ratchet BioniQ
by LASAK s.r.o.
Identity
- Trade Name
- Ratchet BioniQ EUDAMED
- Device Name
- BioniQ Instruments, Non-active non-implantable instruments EUDAMED
- Model / Reference
- Ratchet BioniQ EUDAMED2408.00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 08595573019655 EUDAMED
- Basic UDI-DI
- 85955730006XU EUDAMED
- EMDN Code
- V0399 MEASUREMENT DEVICES - OTHER EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Czechia EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Ratchet BioniQ by LASAK s.r.o. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 85955730006XU | Class I | Active |
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Manufacturer
- Manufacturer
- LASAK s.r.o.
- EUDAMED SRN
- CZ-MF-000031907
Sources (1)
- EUDAMED 447472b5-84ab-4bf9-94bb-28328fc3322b 61 fields · synced Jul 18, 2026