ZEISS CIRRUS HD-OCT 5000 - Indonesia BPOM Medical Device Registration
ZEISS CIRRUS HD-OCT 5000 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201420199. 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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
FLEXTRONIC MANUFACTURING (SINGAPORE) PTE LTDCountry of Origin
Singapore
Authorized Representative
CARL ZEISS NEW ZEISSAR Address
Arkadia Green Park, Tower G 16th Floor, Suite 1608 Jalan TB. Simatupang Kavling 88
Registration Date
Nov 09, 2024
Expiry Date
Sep 30, 2026
Product Type
Diagnostic Eye Equipment
Ophthalmoscope.
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