NUGRA Manifold - Indonesia BPOM Medical Device Registration
NUGRA Manifold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504420156. The device is manufactured by LEPU MEDICAL TECHNOLOGY (BEIJING) CO,. LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LEPU MEDICAL TECHNOLOGY (BEIJING) CO,. LTD.Country of Origin
China
Authorized Representative
PT. NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Oct 30, 2024
Expiry Date
Aug 23, 2027
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
Non Electromedic Sterile
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