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SKINMED® HEALIGHT - Indonesia BPOM Medical Device Registration

SKINMED® HEALIGHT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320692. The device is manufactured by BEIJING LEAD BEAUTY S&T CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.

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
SKINMED® HEALIGHT
Analysis ID: AKL 21403320692

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

HERCA CIPTA DERMAL PERDANA

AR Address

Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460

Registration Date

Aug 01, 2023

Expiry Date

Dec 08, 2027

Product Type

Therapeutic Physical Health Equipment

Infrared lamp.

Non Radiation Electromedics

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