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Compression Therapy Device
EUDAMEDFDA 510(k)Class IIa (EU MDR)
Ref LGT-2210DSModel LGT-2200DVT510(k) K250244
Identity
- Device Name
- Compression Therapy Device EUDAMED
- Model / Reference
- LGT-2200DVT EUDAMEDLGT-2210DS EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06976287180169 EUDAMED
- Basic UDI-DI
- 6976287182200F8 EUDAMED
- EMDN Code
- Z120607 PNEUMATIC COMPRESSION EQUIPMENT EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Spain EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
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
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Compression Therapy Device by Guangzhou Longest Medical Technology Co., Ltd. — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA 510(k)
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K250244 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 6976287182200F8 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Guangzhou Longest Medical Technology Co., Ltd.
- EUDAMED SRN
- CN-MF-000034865
- Authorised Representative
- Lotus NL B.V. NL-AR-000000121
Sources (2)
- EUDAMED b801b590-8845-4751-8b60-8002fb1d721b 85 fields · synced Jun 18, 2026
- FDA 510(k) K250244 1 fields · synced May 19, 2026