Pure Global

DELVI CARE Three Way Stopcock - Indonesia BPOM Medical Device Registration

DELVI CARE Three Way Stopcock is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902420704. The device is manufactured by GUANGDONG BAIHE MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DELVI PRIMATAMA.

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 : C
DELVI CARE Three Way Stopcock
Analysis ID: AKL 20902420704

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DELVI PRIMATAMA

AR Address

Perum Mutiara Gading Timur Blok A8 No. 7-8 RT 001 RW 031 Kelurahan Mustika Jaya, Kecamatan Mustika Jaya - Kota Bekasi

Registration Date

Jul 11, 2024

Expiry Date

Jul 09, 2027

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing