LEICA DM500 and Accessories - Indonesia BPOM Medical Device Registration
LEICA DM500 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420119. The device is manufactured by LEICA MICROSYSTEMS LTD. SHANGHAI from China, 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 MICROSYSTEMS LTD. SHANGHAICountry of Origin
China
Authorized Representative
PT. BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21 RT.002/RW.001 Tanjung Barat, Jagakarsa, Jakarta Selatan, DKI Jakarta
Registration Date
Jul 03, 2024
Expiry Date
Dec 31, 2026
Product Type
Pathology Equipment and Accessories
Microscopes and accessories
Invitro Diagnostics
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