AMPLATZER ™ Guidewire - Indonesia BPOM Medical Device Registration
AMPLATZER ™ Guidewire is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501020891. The device is manufactured by LAKE REGION MEDICAL LIMITED from Ireland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
LAKE REGION MEDICAL LIMITEDCountry of Origin
Ireland
Authorized Representative
NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Jul 27, 2023
Expiry Date
May 31, 2028
Product Type
Diagnostic Cardiology Equipment
Catheter guide wire.
Non Electromedic Sterile
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