Identity
- Trade Name
- ActivForce 2 FDA UDI
- Generic Name
- Electronic goniometer/kinesiology sensor FDA UDI
- Device Name
- Wireless digital dynamometer and goniometer. FDA UDI
- Model / Reference
- Activ5-M FDA UDI
- Description
- Wireless digital dynamometer and goniometer. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850004866184 FDA UDI
- FDA Product Code
- LBB FDA UDIKQX FDA UDI
- GMDN Term
- Electronic goniometer/kinesiology sensor FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 888.1240 FDA UDI888.1500 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: Electronic goniometer/kinesiology sensorBack/leg/chest dynamometer, electronic
ActivForce 2 by Activbody — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Back/leg/chest dynamometer, electronic.
- KINVENT — KINVENT HELLAS · Class II
- KINVENT — KINVENT HELLAS · Class II
- Lafayette Hand-Held Dynamometer — Lafayette Instrument Company · Class I
- KINVENT — KINVENT HELLAS · Class II
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Activbody
Sources (1)
- FDA UDI 5ead61f9-ba17-4bc9-8b78-423de13792ed 34 fields · synced May 30, 2026