NUGRA Manifolds - Indonesia BPOM Medical Device Registration
NUGRA Manifolds is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20504320185. The device is manufactured by SCW MEDICATH 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
SCW MEDICATH LTD.Country of Origin
China
Authorized Representative
PT. NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Aug 17, 2023
Expiry Date
Aug 15, 2026
Product Type
Surgical Cardiology Equipment
Cardiopulmonary bypass adaptor, stopcock, manifold, or fitting.
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