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Echo Static Force Gauge Max

FDA UDI

Class I (US FDA UDI)

by J-Tech Medical, Inc.

Identity

Trade Name
Echo Static Force Gauge Max FDA UDI
Generic Name
Dynamometer force gauge FDA UDI
Device Name
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient. FDA UDI
Model / Reference
RF119 FDA UDI
Description
A device to assist the clinician with establishing an objective assessment of a person’s physical strength. The device is intended to be non-invasive, non-surgical and transient. FDA UDI

Identifiers

Primary DI / UDI-DI
G041RF1190 FDA UDI
FDA Product Code
HRW FDA UDI
GMDN Term
Dynamometer force gauge FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1250 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

No

FDA UDI

Category: Dynamometer force gauge

Echo Static Force Gauge Max by J-Tech Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dynamometer force gauge.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 957d54eb-c846-47b3-958e-8774007fdbe2 34 fields · synced Jun 8, 2026