Identity
- Trade Name
- MAXSO FDA UDI
- Generic Name
- Dental power tool handpiece motorless component FDA UDI
- Device Name
- X92,Contra Angle, 20:1 Implantology, Non-Optic, Push Button, CA Burs FDA UDI
- Model / Reference
- SL3019 FDA UDI
- Description
- X92,Contra Angle, 20:1 Implantology, Non-Optic, Push Button, CA Burs FDA UDI
Identifiers
- Catalog Number
- X92 FDA UDI
- Primary DI / UDI-DI
- 00990010301900 FDA UDI
- FDA Product Code
- EGS FDA UDI
- GMDN Term
- Dental power tool handpiece motorless component FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
MR Safe FDA UDI
Category: Dental power tool handpiece motorless component
Maxso by Beyes Dental Canada Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Beyes Dental Canada Inc
Sources (1)
- FDA UDI 0bd2473e-bdb7-4799-9653-07a98c714773 34 fields · synced Jun 8, 2026