LEICA Surgipath Paraplast - Indonesia BPOM Medical Device Registration
LEICA Surgipath Paraplast is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204220123. The device is manufactured by LEICA BIOSYSTEMS RICHMOND, INC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LEICA BIOSYSTEMS RICHMOND, INCCountry of Origin
United States
Authorized Representative
PT. BIOGEN SCIENTIFICAR Address
Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21
Registration Date
Oct 04, 2023
Expiry Date
Jun 30, 2025
Product Type
Reagents and Specimen Providers
General purpose reagent.
Invitro Diagnostics
LEICA Surgipath™ Decalcifier II
ThermoBrite Slide Denaturation / Hybridization System
ThermoBrite® Slide Denaturation / Hybridization System
LEICA Surgipath Apex BOND Adhesive Slides
LEICA Surgipath EA-50 Modified
LEICA ST Infinity H&E Staining System
LEICA HistoCore Spectra H&E Staining System S1-800
LEICA HistoCore Spectra H&E Staining System S2
LEICA HistoCore Spectra CV X1 Mounting Media
LEICA ST Infinity 2.0 H&E Staining System
LEICA HistoCore PEGASUS Plus and Accessories
LEICA MICROSYSTEMS LTD. SHANGHAI
LEICA HistoCore PEGASUS and Accessories
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LEICA HistoCore Spectra CV and Accessories
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LEICA CM1950 Cryostats and Accessories
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LEICA HistoCore Spectra ST and Accessories
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AIKANG Free Prostate Specific Antigen In Vitro Diagnostic Kit (Chemiluminescent Immunoassay)
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LEICA RM2125 RTS Rotary Microtome and Accessories
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LEICA HistoCore Water Bath M and accessories
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