RESTYLANE Skinboosters Vital Light Lidocaine - Indonesia BPOM Medical Device Registration

RESTYLANE Skinboosters Vital Light Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602122110. The device is manufactured by Q-MED AB from Sweden, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. WICAKSANA OVERSEAS INTERNATIONAL.

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.