LEICA ASP 300S Automated Vacuum Tissue Processor - Indonesia BPOM Medical Device Registration
LEICA ASP 300S Automated Vacuum Tissue Processor is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203013984. The device is manufactured by LEICA BIOSYSTEMS NUSSLOCH GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.
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 : 1
Manufacturer
LEICA BIOSYSTEMS NUSSLOCH GMBH.Country of Origin
Germany
Authorized Representative
PT. BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21
Registration Date
May 10, 2022
Expiry Date
Dec 31, 2023
Product Type
Pathology Equipment and Accessories
Tissue processing equipment (electrically operated)
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