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Chattanooga

FDA UDI

Class II (US FDA UDI)

by Djo, Llc

Identity

Trade Name
CHATTANOOGA FDA UDI
Generic Name
Pneumatic orthopaedic extracorporeal shock wave therapy system FDA UDI
Device Name
RPW V-ACTOR HF HANDPIECE INCL V25 AND V40 TRANSMITTERS FDA UDI
Model / Reference
19365 FDA UDI
Description
RPW V-ACTOR HF HANDPIECE INCL V25 AND V40 TRANSMITTERS FDA UDI

Identifiers

Primary DI / UDI-DI
00190446650973 FDA UDI
FDA Product Code
GZI FDA UDI
GMDN Term
Pneumatic orthopaedic extracorporeal shock wave therapy system 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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Pneumatic orthopaedic extracorporeal shock wave therapy system

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

Similar devices

Also classified as Pneumatic orthopaedic extracorporeal shock wave therapy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Djo, Llc

Sources (1)

  • FDA UDI 7e20f2a2-8075-4926-af61-bf9d33f0c5d5 33 fields · synced May 30, 2026