Identity
- Trade Name
- CHOICE PRO FDA UDI
- Generic Name
- Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
- Device Name
- TDC CHOICE PRO PEDO 5-HOLE FIBER OPTIC HANDPIECE FDA UDI
- Model / Reference
- CP300PL FDA UDI
- Description
- TDC CHOICE PRO PEDO 5-HOLE FIBER OPTIC HANDPIECE FDA UDI
Identifiers
- Catalog Number
- CP300PL FDA UDI
- Primary DI / UDI-DI
- 00810988030933 FDA UDI
- FDA Product Code
- EFB FDA UDI
- GMDN Term
- Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4200 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
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Choice Pro by Handpiece Parts & Repairs, Inc. — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Handpiece Parts & Repairs, Inc.
Sources (1)
- FDA UDI 61e6efbc-f416-4a0c-b8d1-7a15e4ded775 35 fields · synced May 30, 2026