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VENOCHECK Vein Finder - Indonesia BPOM Medical Device Registration

VENOCHECK Vein Finder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903322708. The device is manufactured by QUALMEDI TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FRISMED HOSLAB 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
VENOCHECK Vein Finder
Analysis ID: AKL 10903322708

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. FRISMED HOSLAB INDONESIA

AR Address

Ruko Bidex Blok G No. 30-31 Jl. Pahlawan Seribu BSD City, 15321

Registration Date

Mar 05, 2024

Expiry Date

Jul 15, 2026

Product Type

General Hospital Equipment and Other Individuals

Liquid crystal vein locator

Non Radiation Electromedics

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