NESCO Defibrillator - Indonesia BPOM Medical Device Registration
NESCO Defibrillator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 30505320222. The device is manufactured by SHENZHEN COMEN MEDICAL INSTRUMENT CO.,LTD from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. DJUNIAR & DJUNIAR.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
SHENZHEN COMEN MEDICAL INSTRUMENT CO.,LTDCountry of Origin
China
Authorized Representative
PT. DJUNIAR & DJUNIARAR Address
KOMPLEK RUKAN MAHKOTA ANCOL BLOK D NO.26,JLR.E MARTADINATA ,Desa/Kelurahan Pademangan Barat, Kec.Pademangan,Kota Adm.Jakarta Utara, Provinsi DKI Jakarta. Kode Pos:14420
Registration Date
Jun 02, 2023
Expiry Date
Mar 10, 2026
Product Type
Therapeutic Cardiology Equipment
Automated external defibrillator.
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