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ThermaGuide Cannula for SideLaze800, 150mm
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 100-7014-150
by Cynosure LLC
Identity
- Trade Name
- ThermaGuide Cannula for SideLaze800, 150mm EUDAMEDFDA UDI
- Generic Name
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
- Device Name
- ThermaGuide Cannula for SideLaze800, 150mm EUDAMEDFDA UDI
- Model / Reference
- 100-7014-150 EUDAMEDFDA UDI
- Description
- ThermaGuide Cannula for SideLaze800, 150mm FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00841494100452 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00841494100452 EUDAMED
- 510(k) Number
- K141511 FDA UDI
- FDA Product Code
- GEX FDA UDI
- EMDN Code
- Z12040218 ENDERMOLOGY TREATMENTS EUDAMED
- GMDN Term
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Market of Registration
- Netherlands 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
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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
ThermaGuide Cannula for SideLaze800, 150mm by Cynosure, LLC — Class IIa — 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-00841494100452 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Cynosure LLC
- EUDAMED SRN
- US-MF-000010200
- Authorised Representative
- Cynosure B.V. NL-AR-000009566
Sources (2)
- EUDAMED 447ed402-a594-4f81-b34e-d27d029334a7 61 fields · synced Jul 11, 2026
- FDA UDI fe4f3fd0-8a69-4d03-b1bb-90fd60ed40e1 34 fields · synced May 30, 2026