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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Interferential electrical stimulation system electrode FDA UDI
Device Name
LEGEND XT 4CH STIM PKG US STD FDA UDI
Model / Reference
2786 FDA UDI
Description
LEGEND XT 4CH STIM PKG US STD FDA UDI

Identifiers

Primary DI / UDI-DI
00888912294140 FDA UDI
FDA Product Code
IPF FDA UDI
GMDN Term
Interferential electrical stimulation system electrode 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Interferential electrical stimulation system electrode

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

Similar devices

Also classified as Interferential electrical stimulation 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 5d345230-8061-4b31-820c-f249eb5a625d 33 fields · synced May 31, 2026