JAMILLA Contact Lens - Indonesia BPOM Medical Device Registration
JAMILLA Contact Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204120291. The device is manufactured by I-ZONE from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. KATAMATA.
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
I-ZONECountry of Origin
Korea
Authorized Representative
PT. KATAMATAAR Address
Gedung Delta Building Lt. 1 Jl. Suryopranoto No. 1 Blok A/20
Registration Date
Dec 05, 2024
Expiry Date
Nov 27, 2026
Product Type
Therapeutic Eye Equipment
Soft (hydrophilic) contact lens.
Non Electromedic Sterile
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