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Tixel Periorbital Handpiece
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref MPH00001
by Novoxel Ltd.
Identity
- Trade Name
- Tixel Periorbital Handpiece EUDAMEDTixel-Small Tip Handpiece FDA UDI
- Generic Name
- Thermo-mechanical skin surface treatment system handpiece FDA UDI
- Device Name
- Tixel Periorbital Handpiece EUDAMEDTo be used with Tixel C MSTX0002 Model FDA UDI
- Model / Reference
- MPH00001 EUDAMEDFDA UDI
- Description
- To be used with Tixel C MSTX0002 Model FDA UDI
Identifiers
- Primary DI / UDI-DI
- 07290117520079 EUDAMED07290117524060 FDA UDI
- Basic UDI-DI
- 729011752MPH00001CN EUDAMED
- Direct Marketing DI
- 07290117520079 EUDAMED
- 510(k) Number
- K202988 FDA UDI
- FDA Product Code
- GEI FDA UDI
- EMDN Code
- Z12040203,Z12040218 EUDAMED
- GMDN Term
- Thermo-mechanical skin surface treatment system handpiece FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 878.4400 FDA UDI
- Market of Registration
- Belgium EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Tixel Periorbital Handpiece by Novoxel Ltd — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 729011752MPH00001CN | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Novoxel Ltd.
- EUDAMED SRN
- IL-MF-000008897
- Authorised Representative
- mdi Europa GmbH DE-AR-000006218
Sources (2)
- EUDAMED bd9e1b11-2a1d-4338-8834-7d36906250e7 61 fields · synced Jul 10, 2026
- FDA UDI 527bb612-f9b3-484f-ac71-d916be4e9029 34 fields · synced May 30, 2026