Definisse™ Restore Filler + Lidocaine - Indonesia BPOM Medical Device Registration
Definisse™ Restore Filler + Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602122506. The device is manufactured by CROMA-PHARMA GMBH from Austria, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. TRANSFARMA MEDICA INDAH.
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
CROMA-PHARMA GMBHCountry of Origin
Austria
Authorized Representative
PT. TRANSFARMA MEDICA INDAHAR Address
Unit 802, 8th Fl., Wisma Pondok Indah 2 JL. Sultan Iskandar Muda Kav V - TA, Pondok Indah.
Registration Date
May 05, 2021
Expiry Date
Jul 30, 2025
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
DEFINISSE Hydrobooster
DEFINE Core Filler + Lidocaine
DEFINISSE Restore Filler + Lidocaine
DEFINE Touch Filler + Lidocaine
DEFINE™ Core Filler + Lidocaine
SAYPHA RICH
SAYPHA FILLER
SAYPHA VOLUME
SAYPHA VOLUME PLUS LIDOCAINE
Definisse™ Touch Filler + Lidocaine
DEFINISSE™
ASSUT EUROPE S.P.A
ABBOCATH-T
AMSINO MEDICAL (SHANGHAI) CO., LTD.
QUIXX ™ Sore Throat Spray Kids
VITROBIO SAS
QUIXX ™ Sore Throat Spray
VITROBIO SAS
ATOPICLAIR Cream
BIOKOSMES S.R.L.
DEFINISSE Hydrobooster
CROMA-PHARMA GMBH
DEFINE Core Filler + Lidocaine
CROMA-PHARMA GMBH
DEFINISSE Restore Filler + Lidocaine
CROMA-PHARMA GMBH
DEFINE Touch Filler + Lidocaine
CROMA-PHARMA GMBH
RELIZEMA cream
BIOKOSMES S.R.L

