Identity
- Trade Name
- Patient Interface 125 Kit FDA UDI
- Generic Name
- Laser beam delivery unit holder FDA UDI
- Device Name
- Patient Interface Kit for VICTUS™ Femtosecond Laser Platform (software version 2.7 and higher). Kit consists of Patient Interface 125 and Suction Clip 125. FDA UDI
- Model / Reference
- 1 FDA UDI
- Description
- Patient Interface Kit for VICTUS™ Femtosecond Laser Platform (software version 2.7 and higher). Kit consists of Patient Interface 125 and Suction Clip 125. FDA UDI
Identifiers
- Catalog Number
- 90000115 FDA UDI
- Primary DI / UDI-DI
- 04050555000990 FDA UDI
- FDA Product Code
- HQF FDA UDIOOE FDA UDI
- GMDN Term
- Laser beam delivery unit holder FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 886.4390 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
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
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Patient Interface 125 Kit by Technolas GmbH Perfect Vision — 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
- Technolas GmbH Perfect Vision
Sources (1)
- FDA UDI 7dceb23c-ef0d-4454-916a-938d7d9734e4 37 fields · synced May 30, 2026