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REMEL Salmonella O Factor 8 (Group C2) Agglutinating Serum - Indonesia BPOM Medical Device Registration

REMEL Salmonella O Factor 8 (Group C2) Agglutinating Serum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20303515144. The device is manufactured by REMEL EUROPE LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIPA PUSPA LABSAINS.

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BPOM Registered
Risk Class Kelas Resiko : B
REMEL Salmonella O Factor 8 (Group C2) Agglutinating Serum
Analysis ID: AKL 20303515144

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

REMEL EUROPE LTD.

Country of Origin

United Kingdom

Authorized Representative

PT. DIPA PUSPA LABSAINS

AR Address

Dipa Strategic Office, Lantai Lobby, Jl. Raya Kebayoran Lama No.28 RT.009/RW.011, Kel. Grogol Utara, Kec. Kebayoran Lama

Registration Date

Dec 05, 2023

Expiry Date

Dec 31, 2025

Product Type

Serological Reagents

Salmonella spp. serological reagents.

Invitro Diagnostics

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