Identity
- Trade Name
- Midway Select FDA UDI
- Generic Name
- Dental surgical probe, reusable FDA UDI
- Device Name
- Midway Select Explorer 5 (23/17) Double End Standard Round Handle FDA UDI
- Model / Reference
- 002-0651 FDA UDI
- Description
- Midway Select Explorer 5 (23/17) Double End Standard Round Handle FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00843717108702 FDA UDI
- FDA Product Code
- EKB FDA UDI
- GMDN Term
- Dental surgical probe, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 872.4565 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
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
Yes
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
Midway Select by Midway Dental Supply, Llc — 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
- Midway Dental Supply, Llc
Sources (1)
- FDA UDI f8b32f39-98ec-4136-8202-92ad64c34376 34 fields · synced Jun 6, 2026