Pure Global

GIDCARE Single Use Hypodermic Needle - Indonesia BPOM Medical Device Registration

GIDCARE Single Use Hypodermic Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902221537. The device is manufactured by ANHUI HONGYU WUZHOU MEDICAL MANUFACTURER CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GIDION JAYA.

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
GIDCARE Single Use Hypodermic Needle
Analysis ID: AKL 20902221537

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. GIDION JAYA

AR Address

JL SULTAN HASANUDIN RT 005 / RW 05, AMBON 97128, MALUKU

Registration Date

Dec 31, 2022

Expiry Date

Dec 30, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing