NEUROFORM ATLAS ™ Stent System - Indonesia BPOM Medical Device Registration
NEUROFORM ATLAS ™ Stent System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31002420019. The device is manufactured by STRYKER NEUROVASCULAR from Ireland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
STRYKER NEUROVASCULARCountry of Origin
Ireland
Authorized Representative
NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Feb 21, 2024
Expiry Date
Jun 30, 2025
Product Type
Surgical Neurology Equipment
Neurovascular stent
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