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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Short-wave diathermy treatment system electrode FDA UDI
Device Name
ELECTRODES 80MM CAPACITIVE FDA UDI
Model / Reference
020453216 FDA UDI
Description
ELECTRODES 80MM CAPACITIVE FDA UDI

Identifiers

Primary DI / UDI-DI
00888912187831 FDA UDI
FDA Product Code
IMJ FDA UDI
GMDN Term
Short-wave diathermy treatment system electrode FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5290 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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Short-wave diathermy treatment system electrode

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

Similar devices

Also classified as Short-wave diathermy treatment system electrode.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 1d348538-fc3d-449f-8ea3-038defba3708 33 fields · synced May 29, 2026