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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
NIPRO MEDICAL INDUSTRIES LTD.Country of Origin
Japan
Authorized Representative
SABA INDOMEDIKAAR 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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