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MEDIATECH - MN 01 Mesh Nebulizer - Indonesia BPOM Medical Device Registration

MEDIATECH - MN 01 Mesh Nebulizer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403321825. The device is manufactured by SHENZHEN IMDK MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIA TECHNOLOGY.

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BPOM Registered
Risk Class Kelas Resiko : B
MEDIATECH - MN 01 Mesh Nebulizer
Analysis ID: AKL 20403321825

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDIA TECHNOLOGY

AR Address

KOMPLEK INKOPAL BLOK C NO.71 JL.BOULEVARD BARAT RAYA, KEL.KELAPA GADING

Registration Date

Dec 10, 2023

Expiry Date

Dec 07, 2026

Product Type

Therapeutic Anesthesia Equipment

Nebulizer.

Non Radiation Electromedics

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