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Amnotom 160 Base - Indonesia BPOM Medical Device Registration

Amnotom 160 Base is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421130. The device is manufactured by ALSA APPARECCHI MEDICALI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DUA SRIKANDI INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : C
Amnotom 160 Base
Analysis ID: AKL 21603421130

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

DUA SRIKANDI INDONESIA

AR Address

DUA SRIKANDI INDONESIA

Registration Date

May 29, 2024

Expiry Date

Dec 31, 2026

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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