Identity
- Trade Name
- JAMAR FDA UDI
- Generic Name
- Hand dynamometer/pinchmeter, electronic FDA UDI
- Device Name
- Jamar Smart Hand Dynamometer FDA UDI
- Model / Reference
- 081669928 FDA UDI
- Description
- Jamar Smart Hand Dynamometer FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840216112674 FDA UDI
- FDA Product Code
- HRW FDA UDI
- GMDN Term
- Hand dynamometer/pinchmeter, electronic FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 888.1250 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
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Hand dynamometer/pinchmeter, electronic
Jamar by Asp Global, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Hand dynamometer/pinchmeter, electronic.
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- E-LINK Hand Kit — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Asp Global, LLC
Sources (1)
- FDA UDI 5ba457b5-db52-40c7-8357-f2b985ea2e0f 33 fields · synced May 30, 2026