NEAUVIA Intense Flux - Indonesia BPOM Medical Device Registration
NEAUVIA Intense Flux is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420023. The device is manufactured by MATEX LAB SPA from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.
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
MATEX LAB SPACountry of Origin
Italy
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan
Registration Date
Apr 24, 2024
Expiry Date
Mar 15, 2028
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
TERMOSALUD VMAT PRO
TERMOSALUD
ULTRACOL 200
ULTRA V CO., LTD.
PLASMA IQ Portable Micro Electrosurgery
BERGER & KRAFT MEDICAL SP. ZO.O
LaserMe
BERGER & KRAFT MEDICAL SP. ZO.O.
EpilME
BERGER & KRAFT MEDICAL SP. ZO.O
LIPODEFINE 1470
INTERMEDIC ARFRAN S.A
CRISTAL PRO
DELEO S.A.S
Rigeneracons tube/ devices
HUMAN BRAIN WAVE SRL
S-HEART (Double Arm) Absorbable Polydioxanone Suture
META BIOMED CO., LTD.
BIAXIS Medical Laser Technology Machine QS PICO
HLS HYPERTECH LASER SYSTEMS GMBH

