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Manuthera 242
EUDAMEDFDA UDIClass I (EU MDR)
Ref Manuthera 242Model Manuthera 242 Mobilisation Tables
by Lojer Oy
Identity
- Trade Name
- Manuthera 242 EUDAMEDFDA UDI
- Generic Name
- Examination/treatment table, line-powered FDA UDI
- Device Name
- Treatment table FDA UDI
- Model / Reference
- Manuthera 242 Mobilisation Tables EUDAMEDManuthera 242 EUDAMEDFDA UDI
- Description
- Treatment table FDA UDI
Identifiers
- Catalog Number
- Manuthera 242 FDA UDI
- Primary DI / UDI-DI
- 06430021930668 EUDAMEDFDA UDI
- Basic UDI-DI
- 643002193TT0009W3 EUDAMED
- Direct Marketing DI
- 06430021930668 EUDAMED
- FDA Product Code
- INQ FDA UDI
- EMDN Code
- V0899 MEDICAL SUPPORT EQUIPMENT - OTHER EUDAMED
- GMDN Term
- Examination/treatment table, line-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 890.3760 FDA UDI
- Market of Registration
- Finland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Manuthera 242 by Lojer Oy — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 643002193TT0009W3 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Lojer Oy
- EUDAMED SRN
- FI-MF-000001639
Sources (2)
- EUDAMED fc9dca0f-864e-4f6f-b54c-4de068a50e38 61 fields · synced Jul 12, 2026
- FDA UDI e1a693a2-a19a-4265-8ae7-4425312ae897 36 fields · synced May 30, 2026