LEICA BOND Polymer Refine Detection - Indonesia BPOM Medical Device Registration
LEICA BOND Polymer Refine Detection is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201220113. The device is manufactured by LEICA BIOSYSTEMS MELBOURNE PTY. LTD. from Australia, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is 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 MELBOURNE PTY. LTD.Country of Origin
Australia
Authorized Representative
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
Nov 25, 2024
Expiry Date
Jun 30, 2026
Product Type
Biological Dyes
Immunohistochemistry reagents and kits (Qualitative).
Invitro Diagnostics
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LEICA NOVOCASTRA IHC Diluent
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LEICA NOVOCASTRAโข Novolinkโข Polymer Detection System
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LEICA NOVOCASTRA Epitope Retrieval Solution
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LEICA NOVOCASTRA Epitope Retrieval Solution pH 9 (x10 Concentrate)
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LEICA HistoCore MULTICUT and Accessories
LEICA MICROSYSTEMS LTD. SHANGHAI
LEICA HistoCore BIOCUT and Accessories
LEICA MICROSYSTEMS LTD. SHANGHAI

