ANIOSYME SYNERGY 5 - Indonesia BPOM Medical Device Registration

ANIOSYME SYNERGY 5 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903026678. The device is manufactured by ANIOS LABORATORIES from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PRIMA ALKESINDO NUSANTARA.

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BPOM Registered

Risk Class Kelas Resiko : B

ANIOSYME SYNERGY 5

Analysis ID: AKL 20903026678

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ANIOS LABORATORIES

Country of Origin

France

Authorized Representative

PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

Nov 06, 2020

Expiry Date

Nov 05, 2025

Product Type

General Hospital Equipment and Other Individuals

Liquid chemical sterilants/high level disinfectants.

Non Electromedic Sterile

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