CEREFORM® SILICONE GEL-FILLED BREAST IMPLANTS - Indonesia BPOM Medical Device Registration
CEREFORM® SILICONE GEL-FILLED BREAST IMPLANTS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320230. The device is manufactured by EUROMI BIOSCIENCES from Belgium, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PHARMINDO RHIZOME STURDY.
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
EUROMI BIOSCIENCESCountry of Origin
Belgium
Authorized Representative
PHARMINDO RHIZOME STURDYAR Address
Jalan Arowana No 98 Kel. Kebonagung Kec. Kaliwates
Registration Date
Jul 12, 2023
Expiry Date
Feb 20, 2026
Product Type
Prosthetic Surgical Equipment
Silicone gel-filled breast prosthesis.
Non Electromedic Sterile

