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Rigeneracons tube/ devices - Indonesia BPOM Medical Device Registration

Rigeneracons tube/ devices is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203026071. The device is manufactured by HUMAN BRAIN WAVE SRL from Italy, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : A
Rigeneracons tube/ devices
Analysis ID: AKL 10203026071

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Italy

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Oct 13, 2024

Expiry Date

Jul 08, 2025

Product Type

Pathology Equipment and Accessories

Tissue processing equipment

Invitro Diagnostics

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