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Handpiece cable

FDA UDI

Class II (US FDA UDI)

by Halt Medical, Inc

Identity

Trade Name
Handpiece cable FDA UDI
Generic Name
Electromagnetic surgical navigation device tracking system FDA UDI
Device Name
Cable connects the handpiece to the generator FDA UDI
Model / Reference
4200 FDA UDI
Description
Cable connects the handpiece to the generator FDA UDI

Identifiers

Catalog Number
4200 FDA UDI
Primary DI / UDI-DI
00854763006027 FDA UDI
FDA Product Code
HFG FDA UDI
GMDN Term
Electromagnetic surgical navigation device tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.4160 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Hydrogen Peroxide FDA UDI

Category: Electromagnetic surgical navigation device tracking system

Handpiece cable by Halt Medical, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic surgical navigation device tracking system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Halt Medical, Inc

Sources (1)

  • FDA UDI c9d45f6e-8081-47b8-b711-556855d5e8cf 34 fields · synced May 30, 2026