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AVNER Auto Disable Syringe - Indonesia BPOM Medical Device Registration

AVNER Auto Disable Syringe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902023979. The device is manufactured by GUANGDONG HAIOU MEDICAL APPARATUS CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANUGRAHMITRA IN LINE.

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.

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BPOM Registered
Risk Class Kelas Resiko : B
AVNER Auto Disable Syringe
Analysis ID: AKL 20902023979

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ANUGRAHMITRA IN LINE

AR Address

Jl. Agung Niaga IV Blok G.4 No. 54 Kel. Sunter Agung, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Jul 17, 2020

Expiry Date

Jan 20, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Sterile

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