HEARTSINE Samaritan PAD 500P - Indonesia BPOM Medical Device Registration
HEARTSINE Samaritan PAD 500P is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320256. The device is manufactured by HEARTSINE TECHNOLOGIES, LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. MURSMEDIC.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Risk Classification
Product Class
Kelas : 3
Manufacturer
HEARTSINE TECHNOLOGIES, LTD.Country of Origin
United Kingdom
Authorized Representative
PT. MURSMEDICAR Address
The Kensington Office Tower Lantai 11, Jalan Boulevard Raya Nomor 1, Desa/Kelurahan Kelapa Gading Timur, Kec. Kelapa Gading, Kota Adm. Jakarta Utara, Provinsi DKI Jakarta, 14240
Registration Date
Nov 18, 2024
Expiry Date
May 15, 2028
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
Non Radiation Electromedics
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