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ALMA LASER DermaClear - Indonesia BPOM Medical Device Registration

ALMA LASER DermaClear is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903026365. The device is manufactured by ALMA LASER GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is RADIAN BEAUTIFUL DISTRIVERSA.

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
ALMA LASER DermaClear
Analysis ID: AKL 20903026365

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ALMA LASER GMBH.

Country of Origin

Germany

Authorized Representative

RADIAN BEAUTIFUL DISTRIVERSA

AR Address

KOMPLEKS GRAHA SKG GN BLOK GN NO.5, JL. RAYA KELAPA NIAS

Registration Date

May 29, 2024

Expiry Date

Mar 31, 2028

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus.

Non Radiation Electromedics

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