BARD® MAX-CORE® Disposable Core Biopsy Instrument - Indonesia BPOM Medical Device Registration
BARD® MAX-CORE® Disposable Core Biopsy Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801124274. The device is manufactured by BARD REYNOSA S.A. DE C.V. from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PRO-HEALTH INTERNATIONAL.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
BARD REYNOSA S.A. DE C.V.Country of Origin
Mexico
Authorized Representative
PT. PRO-HEALTH INTERNATIONALAR Address
Komplek Perkantoran Duta Merlin Blok C 35-36 Jalan Gajah Mada 3-5
Registration Date
Jun 23, 2022
Expiry Date
Feb 08, 2027
Product Type
Diagnostic Gastroenterology-Urology Equipment
Gastroenterology-urology biopsy instrument
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