LEICA BOND Primary Antibody Diluent - Indonesia BPOM Medical Device Registration

LEICA BOND Primary Antibody Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10201320820. 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 Primary Antibody Diluent

Analysis ID: AKL 10201320820

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 RT.002/RW.001 Tanjung Barat, Jagakarsa, Jakarta Selatan, DKI Jakarta

Registration Date

Feb 10, 2025

Expiry Date

Jun 30, 2026

Product Type

Biological Dyes

Immunohistochemistry reagents and kits (Qualitative).

Invitro Diagnostics

DJ Fang

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LEICA BOND Primary Antibody Diluent

LEICA BIOSYSTEMS NEWCASTLE LTD.

LEICA BOND Primary Antibody Diluent - 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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