Pure Global

ZEDE Infusion Pump - Indonesia BPOM Medical Device Registration

ZEDE Infusion Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902123968. The device is manufactured by SUZHOU ZEDE MEDICAL INSTRUMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.

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
ZEDE Infusion Pump
Analysis ID: AKL 20902123968

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. DJUNIAR & DJUNIAR

AR Address

KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO. 26

Registration Date

Jul 07, 2021

Expiry Date

Mar 10, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from SUZHOU ZEDE MEDICAL INSTRUMENT CO., LTD
Products from the same manufacturer (1 products)