Auroflex EV Gold - Indonesia BPOM Medical Device Registration
Auroflex EV Gold is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202220058. The device is manufactured by AUROLAB from India, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is MAIN INDEPENDENT MEDEQ.
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
AUROLABCountry of Origin
India
Authorized Representative
MAIN INDEPENDENT MEDEQAR Address
Ruko Graha Mas Pemuda Blok AC-19 jL. Pemuda Blok AC-19 Jl. Pemuda Kel. Jati Kec. Pulo Gadung Jakarta Timur
Registration Date
Sep 28, 2022
Expiry Date
Dec 03, 2025
Product Type
Prosthetic Eye Equipment
Intraocular lens.
Non Electromedic Sterile
ROHTO Visc
FOCUS 8/0 PGA
FOCUS 10/0 Nylon
AUROFLEX
I-VISION Hydrophilic Foldable Poly Hydroxy Ethyl Methacrylate IOL
AUROVISC Hypermellose Ophthalmic Solution
KALVIOL Hydrophilic Aspheric
ROHTO T-BLUE
HUMMINGBIRD Phacoemulsifier
Auro Octane
HAWK i Slitlamp
LABOTECH MICROSCOPES INDIA PVT., LTD.
Auro Octane
AUROLAB
CAT Vision
AUROLAB
AUROLENE Polypropylene Non Absorbable Surgical Needles and Sutures
AUROLAB
TQM Drape Disposable Ophthalmic Drape
OPHTHALMIC TECHNOLOGY
AADI Glaucoma Shunt
AUROLAB
AUROLON Nonabsorbable Surgical Needles and Sutures
AUROLAB
AUROVUE Dfine
AUROLAB

