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VACUETTE Luer Adapter - Indonesia BPOM Medical Device Registration

VACUETTE Luer Adapter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902913250. The device is manufactured by NIPRO MEDICAL INDUSTRIES LTD. from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SABA INDOMEDIKA.

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
VACUETTE Luer Adapter
Analysis ID: AKL 20902913250

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Japan

Authorized Representative

SABA INDOMEDIKA

AR Address

Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9

Registration Date

Apr 30, 2024

Expiry Date

Jul 02, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Intravascular administration set.

Non Electromedic Sterile

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