LEICA BOND Ready-to-Use Primary Antibody Synaptophysin (27G12) - Indonesia BPOM Medical Device Registration

LEICA BOND Ready-to-Use Primary Antibody Synaptophysin (27G12) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201220106. The device is manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BIOGEN SCIENTIFIC.

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BPOM Registered

Risk Class Kelas Resiko : A

LEICA BOND Ready-to-Use Primary Antibody Synaptophysin (27G12)

Analysis ID: AKL 10201220106

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

LEICA BIOSYSTEMS NEWCASTLE LTD

Country of Origin

United Kingdom

Authorized Representative

BIOGEN SCIENTIFIC

AR Address

Rukan Tanjung Mas Raya Jl.Raya Lenteng Agung Blok B1 No.21

Registration Date

Sep 29, 2023

Expiry Date

Jun 30, 2025

Product Type

Biological Dyes

Immunohistochemistry reagents and kits (Qualitative).

Invitro Diagnostics

DJ Fang

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Other Products from LEICA BIOSYSTEMS NEWCASTLE LTD

Products from the same manufacturer (10 products)

LEICA BOND Ready-to-Use Primary Antibody Synaptophysin (27G12) - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

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