← Back to catalogue
LightLas 532/670
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref ML0010Model LightLas 532/670
Identity
- Trade Name
- LightLas 532/670 EUDAMEDFDA UDI
- Generic Name
- Ophthalmic solid-state laser system FDA UDI
- Device Name
- LightLas Pattern Scanning System EUDAMEDThis laser system is included one laser console, laser delivery unit and ophthalmic powered table. There are 3 boxs individually. FDA UDI
- Model / Reference
- LightLas 532/670 EUDAMEDML0010 EUDAMEDFDA UDI
- Description
- This laser system is included one laser console, laser delivery unit and ophthalmic powered table. There are 3 boxs individually. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04712826770659 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04712826770659 EUDAMED
- 510(k) Number
- K103547 FDA UDI
- FDA Product Code
- HQF FDA UDI
- EMDN Code
- Z12011006,Z12011011,Z12011016 EUDAMED
- GMDN Term
- Ophthalmic solid-state laser system FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 886.4390 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
LightLas 532/670 by Lightmed Corporation — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04712826770659 | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Lightmed Corporation
- EUDAMED SRN
- TW-MF-000027493
- Authorised Representative
- MDSS GmbH DE-AR-000005430
Sources (2)
- EUDAMED e77ddd70-0958-410a-a17a-a41fc2b4f2d4 61 fields · synced Jun 18, 2026
- FDA UDI 63882a2d-5da0-44f1-8742-9b4a7d86b426 34 fields · synced May 30, 2026