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Kinvent

FDA UDI

Class II (US FDA UDI)

by Kinvent Hellas

Identity

Trade Name
KINVENT FDA UDI
Generic Name
Hand dynamometer/pinchmeter, electronic FDA UDI
Device Name
Grip is used for the evaluation of hand grip strength. You can assess isometric strength by the way of the peak force as well as of the average force. The Grip dynamometer allows to quantitatively measure the grip weakness caused by injury compared to the strength of the healthy hand FDA UDI
Model / Reference
Grip V2R01 FDA UDI
Description
Grip is used for the evaluation of hand grip strength. You can assess isometric strength by the way of the peak force as well as of the average force. The Grip dynamometer allows to quantitatively measure the grip weakness caused by injury compared to the strength of the healthy hand FDA UDI

Identifiers

Primary DI / UDI-DI
03770011995332 FDA UDI
FDA Product Code
LBB FDA UDI
GMDN Term
Hand dynamometer/pinchmeter, 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: Hand dynamometer/pinchmeter, electronic

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

Similar devices

Also classified as Hand dynamometer/pinchmeter, 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 15093b4a-56d4-4321-bfc1-8956f4e39cbc 35 fields · synced May 30, 2026