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MEDICEL VISCOJECT Injection System - Indonesia BPOM Medical Device Registration

MEDICEL VISCOJECT Injection System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203810469. The device is manufactured by MEDICEL AG. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MAIN INDEPENDENT MEDEQ.

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 : A
MEDICEL VISCOJECT Injection System
Analysis ID: AKL 11203810469

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

MEDICEL AG.

Country of Origin

Switzerland

Authorized Representative

PT. MAIN INDEPENDENT MEDEQ

AR Address

Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur

Registration Date

Mar 07, 2022

Expiry Date

Nov 05, 2026

Product Type

Surgical Eye Equipment

Intraocular lens guide.

Non Electromedic Sterile

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