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HUMAN MEDITEK Plasma Sterilizer - Indonesia BPOM Medical Device Registration

HUMAN MEDITEK Plasma Sterilizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903022449. The device is manufactured by HUMAN MEDITEK CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEGA GLOBAL PRATAMA.

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
HUMAN MEDITEK Plasma Sterilizer
Analysis ID: AKL 20903022449

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MEGA GLOBAL PRATAMA

AR Address

JL. Cengkeh Blok 16 No. 11 Kel. Pinangsia Kec. Tamansari Jakarta Barat 11110

Registration Date

May 07, 2024

Expiry Date

Feb 15, 2027

Product Type

General Hospital Equipment and Other Individuals

Plasma Sterilizer

Non Radiation Electromedics

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