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Aymo

FDA UDI

Class II (US FDA UDI)

by Medical Device Branch of Zhangzhou Easepal Industrial Corporation

Identity

Trade Name
Aymo FDA UDI
Generic Name
Multi-modality skin surface treatment system FDA UDI
Device Name
IPL HAIR REMOVAL DEVICE FDA UDI
Model / Reference
Aymo Beauty D50 148Q-BD50XX-USDG0A FDA UDI
Description
IPL HAIR REMOVAL DEVICE FDA UDI

Identifiers

Primary DI / UDI-DI
06973504240019 FDA UDI
FDA Product Code
OHT FDA UDI
GMDN Term
Multi-modality skin surface treatment system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Multi-modality skin surface treatment system

Aymo by Medical Device Branch of Zhangzhou Easepal Industrial Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Multi-modality skin surface treatment system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Device Branch of Zhangzhou Easepal Industrial Corporation

Sources (1)

  • FDA UDI 229ba507-c012-4ef4-affa-8ad16065d552 33 fields · synced May 31, 2026