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VISCOJECT-BIO 2.2 Injector Set - Indonesia BPOM Medical Device Registration

VISCOJECT-BIO 2.2 Injector Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203120632. The device is manufactured by MEDICEL AT from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ELO KARSA UTAMA.

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
VISCOJECT-BIO 2.2 Injector Set
Analysis ID: AKL 21203120632

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

MEDICEL AT

Country of Origin

Switzerland

Authorized Representative

PT. ELO KARSA UTAMA

AR Address

Jl. Raya Kebayoran Lama No. 34E

Registration Date

Jun 06, 2024

Expiry Date

May 01, 2025

Product Type

Surgical Eye Equipment

Intraocular lens guide

Non Electromedic Sterile

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