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MINIVISC PLUS - Indonesia BPOM Medical Device Registration

MINIVISC PLUS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203320286. The device is manufactured by BOHUS BIOTECH AB from Sweden, and is classified as Risk Class Kelas Resiko : D. 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 : D
MINIVISC PLUS
Analysis ID: AKL 31203320286

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

BOHUS BIOTECH AB

Country of Origin

Sweden

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

Apr 04, 2023

Expiry Date

Dec 19, 2027

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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