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Focused Shock Wave Therapy Device

FDA UDI

Class I (US FDA UDI)

by Guangzhou Longest Medical Technology Co., Ltd.

Identity

Trade Name
Focused Shock Wave Therapy Device FDA UDI
Generic Name
Electromechanical orthopaedic extracorporeal shock wave therapy system FDA UDI
Model / Reference
LGT-2520AP FDA UDI

Identifiers

Primary DI / UDI-DI
06976287180886 FDA UDI
FDA Product Code
ISA FDA UDI
GMDN Term
Electromechanical 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electromechanical orthopaedic extracorporeal shock wave therapy system

Focused Shock Wave Therapy Device by Guangzhou Longest Medical Technology Co., Ltd. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical orthopaedic extracorporeal shock wave therapy system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Guangzhou Longest Medical Technology Co., Ltd.

Sources (1)

  • FDA UDI 96cb8375-7bd0-4374-b36e-78113bec4f67 32 fields · synced Jun 1, 2026