KDL INT Y - Connector Pack - Indonesia BPOM Medical Device Registration
KDL INT Y - Connector Pack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501220084. The device is manufactured by SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTIDAYA MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SHANGHAI KINDLY MEDICAL INSTRUMENTS CO., LTD.Country of Origin
China
Authorized Representative
MULTIDAYA MEDIKAAR Address
RUKAN NIAGA GUNUNG SAHARI BLOK B-1
Registration Date
Feb 25, 2022
Expiry Date
May 01, 2026
Product Type
Diagnostic Cardiology Equipment
Angiographic injector and syringe.
Non Electromedic Sterile
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