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ONIONEX Scalp Vein Set - Indonesia BPOM Medical Device Registration

ONIONEX Scalp Vein Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902122412. The device is manufactured by SHANDONG YIGUANG MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.

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 : C
ONIONEX Scalp Vein Set
Analysis ID: AKL 20902122412

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

May 05, 2021

Expiry Date

Apr 28, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular catheter.

Non Electromedic Sterile

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