LEICA BOND™ CD3 (LN10) - Indonesia BPOM Medical Device Registration

LEICA BOND™ CD3 (LN10) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20201811013. The device is manufactured by LEICA BIOSYSTEMS NEWCASTLE LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. 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.

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BPOM Registered

Risk Class Kelas Resiko : B

LEICA BOND™ CD3 (LN10)

Analysis ID: AKL 20201811013

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

LEICA BIOSYSTEMS NEWCASTLE LTD.

Country of Origin

United Kingdom

Authorized Representative

PT. 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 (Quantitative).

Invitro Diagnostics

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Other Products from LEICA BIOSYSTEMS NEWCASTLE LTD.

Products from the same manufacturer (10 products)

LEICA BOND™ CD3 (LN10) - 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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