Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name: CHATTANOOGA FDA UDI
Generic Name: Analytical non-scalp cutaneous lead FDA UDI
Device Name: CABLE ASSY EMG CH2 FDA UDI
Model / Reference: 27322 FDA UDI
Description: CABLE ASSY EMG CH2 FDA UDI

Identifiers

Primary DI / UDI-DI: 00888912291873 FDA UDI
FDA Product Code: IKD FDA UDI
GMDN Term: Analytical non-scalp cutaneous lead FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 890.1175 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Analytical non-scalp cutaneous lead

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Djo, Llc

Sources (1)

FDA UDI 013a5e2c-add9-458e-ad82-d809792d52d6 33 fields · synced Jun 8, 2026