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VITROLIFE Culture Dish - Indonesia BPOM Medical Device Registration

VITROLIFE Culture Dish is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21105713137. The device is manufactured by HERTART APS. from Denmark, 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
VITROLIFE Culture Dish
Analysis ID: AKL 21105713137

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HERTART APS.

Country of Origin

Denmark

Authorized Representative

PT. DIPA PHARMALAB INTERSAINS

AR Address

Jalan Raya Kebayoran Lama No. 28

Registration Date

Apr 12, 2021

Expiry Date

Nov 11, 2025

Product Type

Reproductive Aids

Assisted reproduction labware.

Invitro Diagnostics

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