Apilus

FDA UDI

Class I (US FDA UDI)

by Dectro International

Identity

Trade Name: Apilus FDA UDI
Generic Name: Professional hair-removal electrolysis system FDA UDI
Device Name: needle-type epilator FDA UDI
Model / Reference: xcell Pro FDA UDI
Description: needle-type epilator FDA UDI

Identifiers

Catalog Number: 01-0605US FDA UDI
Primary DI / UDI-DI: 00686209106059 FDA UDI
FDA Product Code: KCW FDA UDI
GMDN Term: Professional hair-removal electrolysis system FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.5350 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Professional hair-removal electrolysis system

Apilus by Dectro International — 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: Dectro International

Sources (1)

FDA UDI 6d0eff4a-82ea-44d0-b4a9-81cf13032182 34 fields · synced Jun 6, 2026