SAYPHA FILLER - Indonesia BPOM Medical Device Registration
SAYPHA FILLER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602918957. 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. QUALTEK CONSULTANT JAKARTA.
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. QUALTEK CONSULTANT JAKARTAAR Address
Icon Business Park Blok K No 6, BSD City, Kab Tangerang, Banten
Registration Date
Aug 31, 2021
Expiry Date
Aug 30, 2024
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
DEFINE Core Filler + Lidocaine
DEFINISSE Restore Filler + Lidocaine
DEFINE Touch Filler + Lidocaine
DEFINISSE Hydrobooster
DEFINE™ Core Filler + Lidocaine
SAYPHA RICH
SAYPHA VOLUME
SAYPHA VOLUME PLUS LIDOCAINE
Definisse™ Touch Filler + Lidocaine
Definisse™ Restore Filler + Lidocaine
MIACARE DELiGHT 1-Day Silicone Hydrogel Soft Contact Lens
VISCO TECHNOLOGY SDN. BHD.
CUSA Clarity Ultrasonic Surgical Aspirator System
INTEGRA LIFESCIENCES (IRELAND) LIMITED
SAYPHA Filler Lidocaine
CROMA-PHARMA GMBH (CROMAZEILE)
SAYPHA Volume Plus Lidocaine
CROMA-PHARMA GMBH (CROMAZEILE)
SAYPHA Rich
CROMA-PHARMA GMBH (CROMAZEILE)
SAYPHA Volume
CROMA-PHARMA GMBH (CROMAZEILE)
SAYPHA FILLER
CROMA-PHARMA GMBH (CROMAZEILE)
SAYPHA Volume Lidocaine
CROMA-PHARMA GMBH (CROMAZEILE)
Goddess 1 Day Color Contact Lens
YUNG SHENG OPTICAL CO., LTD.
AIRFIT F40
RESMED ASIA PTE., LTD.