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CLEARLIGHT Intense Pulsed Light - Indonesia BPOM Medical Device Registration

CLEARLIGHT Intense Pulsed Light is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403420337. The device is manufactured by EUNSUNG GLOBAL CORP. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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
CLEARLIGHT Intense Pulsed Light
Analysis ID: AKL 21403420337

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. 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 22, 2024

Expiry Date

Mar 14, 2028

Product Type

Therapeutic Physical Health Equipment

Infrared lamp.

Non Radiation Electromedics

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