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OXYTEC Infusion pump - Indonesia BPOM Medical Device Registration

OXYTEC Infusion pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127043. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SANMU HAKARA INDOJAYA.

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BPOM Registered
Risk Class Kelas Resiko : B
OXYTEC Infusion pump
Analysis ID: AKL 20902127043

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. SANMU HAKARA INDOJAYA

AR Address

KOMPLEK PERGUDANGAN ERA PRIMA DAAN MOGOT BLOK L NO.19 JL DAAN MOGOT KM.21 PORIS GAGA BARU, KEL BATU CEPER, KEC. BATU CEPER KOTA TANGERANG

Registration Date

Nov 17, 2021

Expiry Date

Nov 17, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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