Identity
- Trade Name
- Smartlite Pro Endo Activator FDA UDI
- Generic Name
- Solution agitator FDA UDI
- Model / Reference
- 644432 FDA UDI
Identifiers
- Catalog Number
- 644432 FDA UDI
- Primary DI / UDI-DI
- D0016444321 FDA UDI
- FDA Product Code
- EKQ FDA UDI
- GMDN Term
- Solution agitator FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Commercial Distribution
- 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
No
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
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Medical equipment/instrument drape, single-useRoot canal ultrasonic irrigation handpiece tipSolution agitator
Smartlite Pro Endo Activator by Dentsply International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Solution agitator.
- Smartlite Pro Endo Activator — Dentsply International · Class I
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 I | Pending data |
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Manufacturer
- Manufacturer
- Dentsply International
Sources (1)
- FDA UDI 22c215d4-f6bf-4a87-997e-f4f4835895d3 33 fields · synced May 30, 2026