SURPLUG AD Manifold - Indonesia BPOM Medical Device Registration
SURPLUG AD Manifold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902025193. The device is manufactured by TERUMO MEDICAL PRODUCTS (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO MEDICAL PRODUCTS (HANGZHOU) CO., LTD.Country of Origin
China
Authorized Representative
TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Sep 09, 2020
Expiry Date
Jun 05, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular administration set
Non Electromedic Sterile
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