miLOOP - Indonesia BPOM Medical Device Registration
miLOOP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203220051. The device is manufactured by CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
CARL ZEISS MEDITEC CATARACT TECHNOLOGY INC.Country of Origin
United States
Authorized Representative
PT. CARL ZEISS NEW ZEISSAR Address
CARL ZEISS INDONESIA
Registration Date
Jun 30, 2022
Expiry Date
Sep 30, 2026
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Sterile
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