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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Transcutaneous electrical stimulation probe FDA UDI
Device Name
KIT HIVOLT PROBE FDA UDI
Model / Reference
79977 FDA UDI
Description
KIT HIVOLT PROBE FDA UDI

Identifiers

Primary DI / UDI-DI
00888912402996 FDA UDI
FDA Product Code
IPF FDA UDI
GMDN Term
Transcutaneous electrical stimulation probe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5850 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Transcutaneous electrical stimulation probe

Chattanooga by Djo, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Transcutaneous electrical stimulation probe.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 55822c5e-857f-48c1-8e8e-9ee8fa3252dc 33 fields · synced May 30, 2026