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IALURIL Prefill - Indonesia BPOM Medical Device Registration

IALURIL Prefill is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30804220205. The device is manufactured by IBSA FARMACEUTICI ITALIA, SRL from Italy, and is classified as Risk Class Kelas Resiko : D. 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 : D
IALURIL Prefill
Analysis ID: AKL 30804220205

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Italy

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

Jan 13, 2025

Expiry Date

May 17, 2027

Product Type

Gastroenterology-Surgical Urology Equipment

Temporary replacement of glycosaminoglycan layer in the bladder

Non Electromedic Sterile

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