Identity
- Trade Name
- K-Grip EUDAMEDKForce Grip FDA UDI
- Generic Name
- Hand dynamometer/pinchmeter, electronic FDA UDI
- Device Name
- KForce Grip EUDAMEDK 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 K Grip dynamometer allows to quantitatively measure the grip weakness caused by injury compared to the strength of the healthy hand." FDA UDI
- Model / Reference
- MP.04.02.FN EUDAMEDK Grip V3 FDA UDI
- Description
- K 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 K 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
- 03770011995431 EUDAMEDFDA UDI
- Basic UDI-DI
- B-03770011995431 EUDAMED
- FDA Product Code
- LBB FDA UDI
- EMDN Code
- Z120602 PHYSIOTHERAPY EQUIPMENT EUDAMED
- GMDN Term
- Hand dynamometer/pinchmeter, electronic FDA UDI
Classification
- Device Class
- Class I EUDAMEDClass II FDA UDI
- Regulation Number
- 888.1240 FDA UDI
- Market of Registration
- France EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
K-Grip by Kinvent Biomecanique — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-03770011995431 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- KINVENT Biomecanique
- EUDAMED SRN
- FR-MF-000031884
Sources (2)
- EUDAMED 0d01c490-93fb-440d-8845-c99f2359558d 61 fields · synced Jun 18, 2026
- FDA UDI 2785e761-79a8-4671-985f-23f3d5957bac 35 fields · synced May 30, 2026