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GYNETICS I.U.I - Indonesia BPOM Medical Device Registration

GYNETICS I.U.I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21106603833. The device is manufactured by GYNETICS MEDICAL PRODUCTS N.V. from Belgium, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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 : B
GYNETICS I.U.I
Analysis ID: AKL 21106603833

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Belgium

Authorized Representative

PT. DIPA PHARMALAB INTERSAINS

AR Address

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

Registration Date

Oct 16, 2023

Expiry Date

Dec 31, 2025

Product Type

Reproductive Aids

Assisted reproduction microtools.

Non Electromedic Non Sterile

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