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Tixel Handpiece

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref MSH00001

by Novoxel Ltd.

Identity

Trade Name
Tixel Handpiece EUDAMEDFDA UDI
Generic Name
Thermo-mechanical skin surface treatment system handpiece FDA UDI
Device Name
Tixel Handpiece EUDAMED
To be used with Tixel C Model MSTX0002 FDA UDI
Model / Reference
MSH00001 EUDAMEDFDA UDI
Description
To be used with Tixel C Model MSTX0002 FDA UDI

Identifiers

Primary DI / UDI-DI
07290117520062 EUDAMED
07290117524053 FDA UDI
Basic UDI-DI
729011752MSH00001E9 EUDAMED
Direct Marketing DI
07290117520062 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 EUDAMED
Class 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 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

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novoxel Ltd.
EUDAMED SRN
IL-MF-000008897
Authorised Representative
mdi Europa GmbH DE-AR-000006218

Sources (2)

  • EUDAMED 4a7e5699-e485-428d-9ade-2fa8d20e1537 61 fields · synced May 31, 2026
  • FDA UDI 8de120ee-d3ef-4f05-9139-9056024c99b2 34 fields · synced May 29, 2026