← Back to catalogue

Dr.Pen

FDA UDI

Class II (US FDA UDI)

by Guangzhou Ekai Electronic Technology Co., Ltd.

Identity

Trade Name
Dr.Pen FDA UDI
Generic Name
Cosmetic micro-needling electronic handpiece, professional FDA UDI
Model / Reference
A20 FDA UDI

Identifiers

Primary DI / UDI-DI
06976749540012 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
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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
High-level Disinfectant FDA UDI

Category: Cosmetic micro-needling electronic handpiece, professional

Dr.Pen by Guangzhou Ekai Electronic Technology Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cosmetic micro-needling electronic handpiece, professional.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI dffe4d1a-248e-4c33-b551-b4bd62969be8 33 fields · synced May 30, 2026