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Midway Select

FDA UDI

Class I (US FDA UDI)

by Midway Dental Supply, Llc

Identity

Trade Name
Midway Select FDA UDI
Generic Name
Periodontal probe, reusable FDA UDI
Device Name
Midway Select Probe CP12 Single End Color Coded Standard Round Handle FDA UDI
Model / Reference
002-0660 FDA UDI
Description
Midway Select Probe CP12 Single End Color Coded Standard Round Handle FDA UDI

Identifiers

Primary DI / UDI-DI
00843717108795 FDA UDI
FDA Product Code
EIX FDA UDI
GMDN Term
Periodontal probe, reusable 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periodontal probe, reusable

Midway Select by Midway Dental Supply, Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periodontal probe, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 50e23d95-866d-4b93-b307-a24b4e9d8b99 33 fields · synced May 31, 2026