LAPORT Universal Trocar Bladeless Type - Indonesia BPOM Medical Device Registration
LAPORT Universal Trocar Bladeless Type is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10801513590. The device is manufactured by SEJONG MEDICAL CO. LTD. from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SOMETECH NEW Zealand.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SEJONG MEDICAL CO. LTD.Country of Origin
Korea
Authorized Representative
SOMETECH NEW ZealandAR Address
AKR Tower Lantai 11 Unit 11G, Jalan Panjang Nomor 5 RT 011 RW 010
Registration Date
Apr 22, 2019
Expiry Date
Mar 12, 2024
Product Type
Diagnostic Gastroenterology-Urology Equipment
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