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VITROLIFE G-IVF Plus - Indonesia BPOM Medical Device Registration

VITROLIFE G-IVF Plus is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106704861. The device is manufactured by VITROLIFE SWEDEN AB. from Sweden, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is DIPA PHARMALAB INTERSAINS.

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
VITROLIFE G-IVF Plus
Analysis ID: AKL 21106704861

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

DIPA PHARMALAB INTERSAINS

AR Address

Jl. Raya Kebayoran Lama No. 28, Kebayoran Lama,Jakarta Selatan, DKl Jakarta, kode pos : 12210

Registration Date

Aug 02, 2023

Expiry Date

Sep 27, 2027

Product Type

Reproductive Aids

Reproductive media and supplements.

Non Electromedic Sterile

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