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HETTICH Rotosilenta 630 RS Centrifuge - Indonesia BPOM Medical Device Registration

HETTICH Rotosilenta 630 RS Centrifuge is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209020890. The device is manufactured by ANDREAS HETTICH GMBH & CO, KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PRIMA ALKESINDO NUSANTARA.

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 : C
HETTICH Rotosilenta 630 RS Centrifuge
Analysis ID: AKL 20209020890

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PRIMA ALKESINDO NUSANTARA

AR Address

Jl. Bukit Gading Raya Blok C 12 - C 15 Kel. Kelapa Gading Barat, Kec. Kelapa Gading, Jakarta Utara

Registration Date

Mar 08, 2024

Expiry Date

Jan 25, 2029

Product Type

Products used in the manufacture of blood preparations and preparations of origin and blood

Automated cell-washing centrifuge for immuno-hematology.

Invitro Diagnostics

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