NUGRA Guide Wire - Indonesia BPOM Medical Device Registration
NUGRA Guide Wire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501320909. The device is manufactured by SCW MEDICATH LTD. from China, and is classified as Risk Class Kelas Resiko : C. 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
Jul 26, 2023
Expiry Date
May 22, 2026
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
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