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CLEA Laser Therapy Device - Indonesia BPOM Medical Device Registration

CLEA Laser Therapy Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403220314. The device is manufactured by WUHAN GUANGDUN TECHNOLOGY CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. VERIMARK.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
CLEA Laser Therapy Device
Analysis ID: AKL 21403220314

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. VERIMARK

AR Address

Komplek Roxy Mas Blok E2 No. 20 Jl. KH. Hasyim Ashari 125 Kel. Cideng Kec. Gambir Jakarta Pusat 10150

Registration Date

Nov 18, 2022

Expiry Date

Feb 22, 2027

Product Type

Therapeutic Physical Health Equipment

Infrared lamp.

Non Radiation Electromedics

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