Identity
- Trade Name
- Footswitch FDA UDI
- Generic Name
- Cosmetic micro-needling electronic handpiece, professional FDA UDI
- Device Name
- Box of Footswitch. The Footswitch is an accessory of Exceed AD61USMP. FDA UDI
- Model / Reference
- E100201USMP FDA UDI
- Description
- Box of Footswitch. The Footswitch is an accessory of Exceed AD61USMP. FDA UDI
Identifiers
- Catalog Number
- E100201USMP FDA UDI
- Primary DI / UDI-DI
- EMTDE100201USMP1 FDA UDI
- FDA Product Code
- QAI FDA UDI
- GMDN Term
- Cosmetic micro-needling electronic handpiece, professional FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 878.4430 FDA UDI
- Commercial Distribution
- Not 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
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Footswitch by MT.DERM GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- MT.DERM GmbH
Sources (1)
- FDA UDI 16658634-77d4-4aba-b540-487520eb1496 36 fields · synced May 30, 2026