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MAQUET PowerLED II Range - Indonesia BPOM Medical Device Registration

MAQUET PowerLED II Range is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603126418. The device is manufactured by MAQUET SAS from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is INDOSOPHA SAKTI.

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BPOM Registered
Risk Class Kelas Resiko : B
MAQUET PowerLED II Range
Analysis ID: AKL 21603126418

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MAQUET SAS

Country of Origin

France

Authorized Representative

INDOSOPHA SAKTI

AR Address

Jl.Mampang Prapatan Raya No.1

Registration Date

Dec 23, 2022

Expiry Date

Dec 31, 2024

Product Type

Surgical Equipment

Surgical lamp.

Non Radiation Electromedics

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