Pure Global

VIDA Suction Catheter - Indonesia BPOM Medical Device Registration

VIDA Suction Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20404420094. The device is manufactured by WELL LEAD MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DANVI MEDILAB PERKASA.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
VIDA Suction Catheter
Analysis ID: AKL 20404420094

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DANVI MEDILAB PERKASA

AR Address

Jl. Kapten Muslim Komp. Mega Com Center Blok G No. 1-2 Kel. Dwikora Kec. Medan Helvetia

Registration Date

Aug 04, 2024

Expiry Date

Jan 30, 2026

Product Type

Other Anesthesia Equipment

Tracheobroncial Suction Catheter

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing