OLYMPUS Single Use Ligating Device - Indonesia BPOM Medical Device Registration
OLYMPUS Single Use Ligating Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804024635. The device is manufactured by AOMORI OLYMPUS CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURSMEDIC.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
AOMORI OLYMPUS CO., LTD.Country of Origin
Japan
Authorized Representative
PT. MURSMEDICAR Address
Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat
Registration Date
Mar 27, 2023
Expiry Date
Mar 31, 2025
Product Type
Gastroenterology-Surgical Urology Equipment
Hemorrhoidal ligator.
Non Electromedic Sterile
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