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VADI Water Trap - Indonesia BPOM Medical Device Registration

VADI Water Trap is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403022170. The device is manufactured by VADI MEDICAL TECHNOLOGY CO. LTD. from Taiwan (China), and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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
VADI Water Trap
Analysis ID: AKL 10403022170

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Taiwan (China)

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Apr 20, 2020

Expiry Date

Jan 01, 2025

Product Type

Therapeutic Anesthesia Equipment

Anesthesia breathing circuit.

Non Electromedic Non Sterile

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