Identity
- Trade Name
- microfet3 FDA UDI
- Generic Name
- Dynamometer force gauge FDA UDI
- Device Name
- The microFET®3 is a dynamometer device for performing muscle tests to quantitatively measure muscle weakness caused by injury or disease, as well as measure general muscle strength. The device is used to record and convey an individual's ability to resist force for a specific muscle or muscle group being tested. Range of motion tests to quantitatively measure the angle of the body segment or joint tested to determine an individual's range of motion referenced from body's natural position. FDA UDI
- Model / Reference
- 5026 FDA UDI
- Description
- The microFET®3 is a dynamometer device for performing muscle tests to quantitatively measure muscle weakness caused by injury or disease, as well as measure general muscle strength. The device is used to record and convey an individual's ability to resist force for a specific muscle or muscle group being tested. Range of motion tests to quantitatively measure the angle of the body segment or joint tested to determine an individual's range of motion referenced from body's natural position. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850002429312 FDA UDI
- FDA Product Code
- LBB FDA UDI
- GMDN Term
- Dynamometer force gauge 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: Dynamometer force gauge
microfet3 by Hoggan Scientific L.L.C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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
- Hoggan Scientific L.L.C.
Sources (1)
- FDA UDI 213d1692-695a-4171-aa42-3c8ef777d182 33 fields · synced Jun 8, 2026