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Chattanooga

FDA UDI

Class I (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
FALCON RPW HANDPIECE - G2 FDA UDI
Model / Reference
48080-R FDA UDI
Description
FALCON RPW HANDPIECE - G2 FDA UDI

Identifiers

Primary DI / UDI-DI
00190446887225 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Pneumatic orthopaedic extracorporeal shock wave therapy system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5660 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Pneumatic orthopaedic extracorporeal shock wave therapy system

Chattanooga by Djo, Llc — Class I — 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 51804c37-30a0-4e56-ac98-a6ba86d50b77 33 fields · synced Jun 1, 2026