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Kinvent

FDA UDI

Class II (US FDA UDI)

by Kinvent Hellas

Identity

Trade Name
KINVENT FDA UDI
Generic Name
Back/leg/chest dynamometer, electronic FDA UDI
Device Name
Link is a traction dynamometer for the measurement of isometric strength and biofeedback training. Link enables independent measurements. It can be fixed on a physiotherapists table, on the espalier or on pulley machines. FDA UDI
Model / Reference
Link V2R01 FDA UDI
Description
Link is a traction dynamometer for the measurement of isometric strength and biofeedback training. Link enables independent measurements. It can be fixed on a physiotherapists table, on the espalier or on pulley machines. FDA UDI

Identifiers

Primary DI / UDI-DI
03770011995004 FDA UDI
FDA Product Code
LBB FDA UDI
GMDN Term
Back/leg/chest dynamometer, electronic FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.1240 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Back/leg/chest dynamometer, electronic

Kinvent by Kinvent Hellas — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Back/leg/chest dynamometer, electronic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kinvent Hellas

Sources (1)

  • FDA UDI 27341b41-d05c-40c9-9886-aed72ca6cf66 35 fields · synced May 30, 2026