Identity
- Trade Name
- Waterlase Laser Tips - Sapphire EUDAMEDWaterlase Laser Tips FDA UDI
- Generic Name
- Dental solid-state laser system FDA UDI
- Device Name
- WaterLase Laser Tips, MX5/ MX7, Turbo, 2PK EUDAMEDA tip kit containing 2 reusable laser tips intended for use with Waterlase laser systems. The tips have the same length of 2 mm and vary in core diameter. FDA UDI
- Model / Reference
- 7200406 EUDAMEDMX Turbo Tips FDA UDI
- Description
- A tip kit containing 2 reusable laser tips intended for use with Waterlase laser systems. The tips have the same length of 2 mm and vary in core diameter. FDA UDI
Identifiers
- Catalog Number
- 7200406 FDA UDI
- Primary DI / UDI-DI
- 00647529001622 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00647529001622 EUDAMED
- 510(k) Number
- K090181 FDA UDI
- FDA Product Code
- GEX FDA UDI
- EMDN Code
- Z12011099 LASER SURGERY INSTRUMENTS - OTHER EUDAMED
- GMDN Term
- Dental solid-state laser system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4810 FDA UDI
- Market of Registration
- Germany 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
Yes
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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Dimensions & Sizes
- Size
- Outer Diameter — 700 Micrometer FDA UDIOuter Diameter — 500 Micrometer FDA UDILength — 2 Millimeter FDA UDI
Waterlase Laser Tips - Sapphire by Biolase Mg 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-00647529001622 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Biolase Mg Llc
- EUDAMED SRN
- US-MF-000028587
- Authorised Representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Sources (2)
- EUDAMED 5fe1448a-e31a-44c1-b7d7-ce366ae086e2 61 fields · synced Jun 18, 2026
- FDA UDI abef6ee3-edd9-4f7e-8505-b6a5ecfe55a2 37 fields · synced May 30, 2026