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AMSCO® V-PROTM Max Single Door Low Temperature Sterilization System - Indonesia BPOM Medical Device Registration

AMSCO® V-PROTM Max Single Door Low Temperature Sterilization System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903712895. The device is manufactured by STERIS MEXICO. S. DE R.L DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOMEDIK NIAGA PERKASA.

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 : B
AMSCO® V-PROTM Max Single Door Low Temperature Sterilization System
Analysis ID: AKL 20903712895

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

PT. INDOMEDIK NIAGA PERKASA

AR Address

Ruko Cempaka Mas Blok N No. 29 Jl. Letjend R. Suprapto, Kemayoran Jakarta Pusat

Registration Date

Dec 23, 2021

Expiry Date

Aug 19, 2026

Product Type

General Hospital Equipment and Other Individuals

Steam sterilizer.

Non Radiation Electromedics

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