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GERMITEC Antigermix E1 - Indonesia BPOM Medical Device Registration

GERMITEC Antigermix E1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903912968. The device is manufactured by GERMITEC from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.

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
GERMITEC Antigermix E1
Analysis ID: AKL 20903912968

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GERMITEC

Country of Origin

France

Authorized Representative

PT. MURSMEDIC

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

Mar 10, 2022

Expiry Date

Nov 27, 2026

Product Type

General Hospital Equipment and Other Individuals

Ultraviolet (UV) radiation chamber disinfection device

Non Radiation Electromedics

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