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MORPHEUS ND HYBRID - Indonesia BPOM Medical Device Registration

MORPHEUS ND HYBRID is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403125092. The device is manufactured by SIARE ENGINERING INTERNATIONAL GROUP S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GLOBAL MEDICAL PRESS.

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BPOM Registered
Risk Class Kelas Resiko : C
MORPHEUS ND HYBRID
Analysis ID: AKL 20403125092

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. GLOBAL MEDICAL PRESS

AR Address

Kompl.Green Garden AA-1/17 Jl.MH Thamrin KM 7 RT 04/RW 02 Kel.Panunggangan Utara Kec.Pinang.Kota Tangerang

Registration Date

Sep 08, 2021

Expiry Date

Jun 23, 2025

Product Type

Therapeutic Anesthesia Equipment

Gas machine for anesthesia or analgesia.

Non Radiation Electromedics

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