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Bifurcated Probe

FDA UDI

Class II (US FDA UDI)

by Kerr Corporation

Identity

Trade Name
Bifurcated Probe FDA UDI
Generic Name
Endodontic apex locator FDA UDI
Device Name
Bifurcated Probe FDA UDI
Model / Reference
973-0307 FDA UDI
Description
Bifurcated Probe FDA UDI

Identifiers

Primary DI / UDI-DI
00195062031083 FDA UDI
FDA Product Code
EAT FDA UDI
GMDN Term
Endodontic apex locator FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1720 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

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: Endodontic apex locator

Bifurcated Probe by Kerr Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic apex locator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kerr Corporation

Sources (1)

  • FDA UDI 50fc4400-974f-4305-b0e1-30d5841584fd 34 fields · synced Jun 8, 2026