Identity
- Trade Name
- FeetMe Monitor Charging Case FTM-DK-CC FDA UDI
- Generic Name
- Noninvasive device battery charger FDA UDI
- Device Name
- This device is a charging and transportation case for up to 12 pair of FTM-DK insoles FDA UDI
- Model / Reference
- V1 FDA UDI
- Description
- This device is a charging and transportation case for up to 12 pair of FTM-DK insoles FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03760349820109 FDA UDI
- FDA Product Code
- JFC FDA UDI
- GMDN Term
- Noninvasive device battery charger FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.1600 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: Noninvasive device battery charger
FeetMe Monitor Charging Case FTM-DK-CC by Feetme — Class I — 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 I | Pending data |
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Manufacturer
- Manufacturer
- Feetme
Sources (1)
- FDA UDI 8e46dd93-6204-43b9-94e1-7e2c21b3f7df 34 fields · synced May 31, 2026