Identity
- Trade Name
- LAMEVEN Eye Massager FDA UDI
- Generic Name
- Eyelid massager FDA UDI
- Model / Reference
- MD-206 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06975977230016 FDA UDI
- FDA Product Code
- ISA FDA UDI
- GMDN Term
- Eyelid massager FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5660 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
LAMEVEN Eye Massager by Dongguan City Umed Technology Co., Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Dongguan City Umed Technology Co., Ltd
Sources (1)
- FDA UDI c370538a-d752-4079-b99a-e90de0466224 33 fields · synced May 30, 2026