Identity
- Trade Name
- SurgiTouch™ Scanner FDA UDI
- Generic Name
- Surgical laser system beam-focus handpiece FDA UDI
- Model / Reference
- kit for AcuPulse and AcuPulse DUO FDA UDI
Identifiers
- Catalog Number
- KT-1000100 FDA UDI
- Primary DI / UDI-DI
- 07290109142203 FDA UDI
- FDA Product Code
- GEX FDA UDI
- GMDN Term
- Surgical laser system beam-focus handpiece FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4810 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
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
SurgiTouch™ Scanner by Lumenis — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Lumenis
Sources (1)
- FDA UDI 3a6faa70-c8ec-4a24-82a6-5c11a1f47c8a 35 fields · synced Jun 1, 2026