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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Physical therapy transcutaneous electrical stimulation system, line-powered FDA UDI
Device Name
VECTRA GENISYS 2CH COMBO PKG US STD, 5CM APPL FDA UDI
Model / Reference
2761 FDA UDI
Description
VECTRA GENISYS 2CH COMBO PKG US STD, 5CM APPL FDA UDI

Identifiers

Primary DI / UDI-DI
00888912292849 FDA UDI
FDA Product Code
GZI FDA UDI
GMDN Term
Physical therapy transcutaneous electrical stimulation system, line-powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.5810 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Physical therapy transcutaneous electrical stimulation system, line-powered

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

Similar devices

Also classified as Physical therapy transcutaneous electrical stimulation system, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI ce7646ad-d3f6-4adb-910f-c73b508cd95e 33 fields · synced May 31, 2026