AT TORBI 719 - Indonesia BPOM Medical Device Registration
AT TORBI 719 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202520001. The device is manufactured by CARL ZEISS MEDITEC AG from Germany, and is classified as Risk Class Kelas Resiko : D. 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.
Risk Classification
Product Class
Kelas : 3
Manufacturer
CARL ZEISS MEDITEC AGCountry of Origin
Germany
Authorized Representative
CARL ZEISS NEW ZEISSAR Address
Arkadia Green Park, Tower G 16th Floor, Suite 1608 Jalan TB. Simatupang Kavling 88
Registration Date
Jan 03, 2025
Expiry Date
Jan 17, 2029
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
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