Identity
- Trade Name
- microfet handgrip FDA UDI
- Generic Name
- Hand dynamometer/pinchmeter, electronic FDA UDI
- Device Name
- The microFET® handGRIP is a dynamometer device for performing muscle grip strength tests to quantitatively measure muscle weakness caused by injury or disease, as well as measure general muscle strength of hand. FDA UDI
- Model / Reference
- 5050-100 FDA UDI
- Description
- The microFET® handGRIP is a dynamometer device for performing muscle grip strength tests to quantitatively measure muscle weakness caused by injury or disease, as well as measure general muscle strength of hand. FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850002429114 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
microfet handgrip by Hoggan Scientific L.L.C. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Hand dynamometer/pinchmeter, electronic.
- JAMAR — Asp Global, LLC · Class I
- Echo Grip Gauge — J-Tech Medical, Inc. · Class I
- DualGrip Digital Grip Dynamometer — Lafayette Instrument Company · Class I
- Biometrics Ltd Dynamometer — BIOMETRICS LIMITED · Class II
- Eforto — Uniweb · Class II
- Northstar Echo Grip Gauge — J-Tech Medical, Inc. · Class I
- E-LINK Hand Kit — BIOMETRICS LIMITED · Class II
- Biometrics Ltd Pinchmeter — BIOMETRICS LIMITED · 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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Hoggan Scientific L.L.C.
Sources (1)
- FDA UDI 5a1c6c3c-afba-4a18-9ef1-7397bdc9d831 33 fields · synced May 30, 2026