PRO-TOUCH Vectra Diode laser system - Indonesia BPOM Medical Device Registration
PRO-TOUCH Vectra Diode laser system is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603918361. The device is manufactured by XINTEC CORPORATION DBA CONVERGENT LASER TECHNOLOGIES from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is SIGMA KARSA MAGNA.
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
Country of Origin
United States
Authorized Representative
SIGMA KARSA MAGNAAR Address
Ruko Mega Grosir Cempaka Mas, Jl. Letjen Suprapto Blok J No. 37-38 RW.08, Kel. Sumur Batu, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta
Registration Date
Sep 07, 2023
Expiry Date
Sep 30, 2027
Product Type
Surgical Equipment
Laser surgical instrument for use in general and plastic surgery and in dermatology.
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