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CARLO Alu Comfort EP 185
EUDAMEDFDA UDIClass I (EU MDR)
Ref K120 BEKA Lifter und deren Zubehör
Identity
- Trade Name
- CARLO Alu Comfort EP 185 EUDAMEDCarlo Alu Comfort EP Patient Lift FDA UDI
- Generic Name
- Mobile patient lifting system, electrically-powered FDA UDI
- Device Name
- CARLO Alu Classic 185 EUDAMEDCarlo Alu Comfort EP Patient Lift FDA UDI
- Model / Reference
- K120 BEKA Lifter und deren Zubehör EUDAMED925006018 FDA UDI
- Description
- Carlo Alu Comfort EP Patient Lift FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04260735022432 EUDAMEDFDA UDI04260735020803 EUDAMED04260735020780 EUDAMED04260735020728 EUDAMED04260735020773 EUDAMED04260735020766 EUDAMED
- Basic UDI-DI
- 426068189120BM EUDAMED
- Direct Marketing DI
- 04260735022432 EUDAMED04260735020803 EUDAMED04260735020780 EUDAMED04260735020728 EUDAMED04260735020773 EUDAMED04260735020766 EUDAMED
- FDA Product Code
- FSA FDA UDI
- EMDN Code
- V0805030102 ELECTRIC MOBILE LIFTS EUDAMED
- GMDN Term
- Mobile patient lifting system, electrically-powered FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 880.5510 FDA UDI
- Market of Registration
- Germany 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
Yes
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
No
FDA UDI
CARLO Alu Comfort EP 185 by BEKA Hospitec GmbH — 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 | 426068189120BM | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- BEKA-Hospitec GmbH
- EUDAMED SRN
- DE-MF-000013895
Sources (7)
- EUDAMED 3a87ddd3-207b-49f0-888c-296f780b96bd 61 fields · synced Oct 6, 2026
- EUDAMED dfe359be-1b5a-45ec-ab94-7cf8380a5984 61 fields · synced May 17, 2026
- EUDAMED 489778fe-e53c-4423-bb38-738c837c6737 61 fields · synced May 17, 2026
- EUDAMED 5082646f-5c75-4ee7-8b68-0c1296163b1e 61 fields · synced May 19, 2026
- EUDAMED 19b40fa5-52e0-4f1a-9d24-48ed7a8ce710 61 fields · synced May 19, 2026
- EUDAMED 5343018c-d353-41ea-88fb-9806f2bc7154 61 fields · synced May 19, 2026
- FDA UDI 1ae9bc38-321f-4155-aedd-8cca64c6913f 33 fields · synced May 30, 2026