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LEICA Bond Max and Accessories - Indonesia BPOM Medical Device Registration

LEICA Bond Max and Accessories is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20203911961. The device is manufactured by LEICA BIOSYSTEMS MELBOURNE PTY. LTD. from Australia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BIOGEN SCIENTIFIC.

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BPOM Registered
Risk Class Kelas Resiko : B
LEICA Bond Max and Accessories
Analysis ID: AKL 20203911961

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Australia

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

Dec 02, 2024

Expiry Date

Jun 30, 2026

Product Type

Pathology Equipment and Accessories

Automated slide stainer.

Invitro Diagnostics

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