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LEICA DM500 and Accessories - Indonesia BPOM Medical Device Registration

LEICA DM500 and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203420119. The device is manufactured by LEICA MICROSYSTEMS LTD. SHANGHAI from China, and is classified as Risk Class Kelas Resiko : A. 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 : A
LEICA DM500 and Accessories
Analysis ID: AKL 10203420119

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

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

Jul 03, 2024

Expiry Date

Dec 31, 2026

Product Type

Pathology Equipment and Accessories

Microscopes and accessories

Invitro Diagnostics

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