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8mm-Zoom-Collimated handpiece (Tip type: Stick type)
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref HOLLYWOOD SPECTRA
Identity
- Trade Name
- 8mm-Zoom-Collimated handpiece (Tip type: Stick type) EUDAMEDHOLLYWOOD SPECTRA FDA UDI
- Generic Name
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
- Device Name
- Frequency Doubled Q-switched Nd-YAG Laser system EUDAMED8mm-Zoom-Collimated Handpiece FDA UDI
- Model / Reference
- HOLLYWOOD SPECTRA EUDAMED8mm-Zoom-Collimated Handpiece FDA UDI
- Description
- 8mm-Zoom-Collimated Handpiece FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809447654751 EUDAMEDFDA UDI
- Basic UDI-DI
- 88094476510118AVX EUDAMED
- FDA Product Code
- GEX FDA UDI
- EMDN Code
- Z12011017 NEODYMIUM SURGICAL LASER EUDAMED
- GMDN Term
- General/multiple surgical frequency-doubled solid-state laser system FDA UDI
Classification
- Device Class
- Class IIb 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
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
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
8mm-Zoom-Collimated handpiece (Tip type: Stick type) by Lutronic Corporation — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID
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 | 88094476510118AVX | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Lutronic Corporation
- EUDAMED SRN
- KR-MF-000009035
- Authorised Representative
- Emergo Europe B.V. NL-AR-000000116
Sources (2)
- EUDAMED 2e788d9d-997d-41e6-879a-058788cc88c7 61 fields · synced Jul 22, 2026
- FDA UDI 29796c33-c109-4228-bb8d-66928a2ea70d 35 fields · synced May 30, 2026