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BIOBASE Vein Finder - Indonesia BPOM Medical Device Registration

BIOBASE Vein Finder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903421117. The device is manufactured by BIOBASE BIODAITECH (SHANDONG) CO, LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. HAS PUTRA INDONESIA.

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 : A
BIOBASE Vein Finder
Analysis ID: AKL 10903421117

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. HAS PUTRA INDONESIA

AR Address

JL.PAL PUTIH NO.72

Registration Date

Nov 18, 2024

Expiry Date

May 16, 2027

Product Type

General Hospital Equipment and Other Individuals

Liquid crystal vein locator

Non Radiation Electromedics

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