BOECO REFRIGERATED CENTRIFUGE M-240R - Indonesia BPOM Medical Device Registration

BOECO REFRIGERATED CENTRIFUGE M-240R is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10205026185. The device is manufactured by ANDREAS HETTICH GMBH + CO. KG, from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BAVARIA COMBININDO.

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.