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ONIONEX Infusion Set for Pediatric - Indonesia BPOM Medical Device Registration

ONIONEX Infusion Set for Pediatric is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902121148. 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.

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BPOM Registered
Risk Class Kelas Resiko : C
ONIONEX Infusion Set for Pediatric
Analysis ID: AKL 20902121148

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

Mar 03, 2021

Expiry Date

Mar 02, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

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