ZEISS CLARUS 700 - Indonesia BPOM Medical Device Registration

ZEISS CLARUS 700 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420189. The device is manufactured by FLEXTRONIC MANUFACTURING (SINGAPORE) PTE., LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CARL ZEISS NEW ZEISS.

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.