LEUKOMED SORBACT - Indonesia BPOM Medical Device Registration
LEUKOMED SORBACT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603917013. The device is manufactured by PLASTOD SPA from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ESSITY HYGIENE AND HEALTH INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PLASTOD SPACountry of Origin
Italy
Authorized Representative
PT. ESSITY HYGIENE AND HEALTH INDONESIAAR Address
Green Office Park 6, Wing B, lantai 1, Zona 8-12, BSD Green Office Park, BSD City, Desa Sampora, Kec. Cisauk, Kab.Tangerang 15345
Registration Date
Oct 06, 2023
Expiry Date
Feb 06, 2025
Product Type
Surgical Equipment
Nonresorbable gauze/sponge for external use, non sterile
Non Electromedic Sterile
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