SAYPHA VOLUME - Indonesia BPOM Medical Device Registration
SAYPHA VOLUME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602020077. 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.
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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 30, 2021
Expiry Date
Aug 30, 2024
Product Type
Prosthetic Surgical Equipment
Dermal filler
Non Electromedic Sterile
DEFINE Touch Filler + Lidocaine
DEFINISSE Hydrobooster
DEFINE Core Filler + Lidocaine
DEFINISSE Restore Filler + Lidocaine
DEFINE™ Core Filler + Lidocaine
SAYPHA FILLER
SAYPHA RICH
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.