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GRINMED Breathing System Filter - Indonesia BPOM Medical Device Registration

GRINMED Breathing System Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321822. The device is manufactured by CREATE BIOTECH CO., LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HARMONY MEDICI INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : B
GRINMED Breathing System Filter
Analysis ID: AKL 20403321822

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Taiwan (China)

Authorized Representative

HARMONY MEDICI INDONESIA

AR Address

KOMPLEK PERUM TAMAN PALEM LESTARI BLOK P NO. 21

Registration Date

Dec 10, 2023

Expiry Date

Dec 07, 2026

Product Type

Therapeutic Anesthesia Equipment

Breathing circuit bacterial filter.

Non Electromedic Non Sterile

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