Pure Global

ZONTIC Disposable Fistula Needles - Indonesia BPOM Medical Device Registration

ZONTIC Disposable Fistula Needles is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805122620. 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 KARINDO ALKESTRON.

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
ZONTIC Disposable Fistula Needles
Analysis ID: AKL 20805122620

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

KARINDO ALKESTRON

AR Address

JL. TOMANG RAYA NO.17

Registration Date

Mar 13, 2024

Expiry Date

Mar 11, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Hemodialysis system and accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing