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HEPASHOT - Indonesia BPOM Medical Device Registration

HEPASHOT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801915134. The device is manufactured by VIGEO S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BRIDGE TWO.

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
HEPASHOT
Analysis ID: AKL 20801915134

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VIGEO S.R.L

Country of Origin

Italy

Authorized Representative

BRIDGE TWO

AR Address

Jl. Petojo Melintang No. 17

Registration Date

Aug 02, 2023

Expiry Date

Jan 09, 2028

Product Type

Diagnostic Gastroenterology-Urology Equipment

Gastroenterology-urology biopsy instrument

Non Electromedic Sterile

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