SkinFuse Lift HG - Indonesia BPOM Medical Device Registration
SkinFuse Lift HG is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324608. The device is manufactured by BIOMED LABORATORIES, LLC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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 : 2
Manufacturer
BIOMED LABORATORIES, LLCCountry of Origin
United States
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Aug 07, 2023
Expiry Date
Jan 01, 2028
Product Type
Surgical Equipment
Hydrogel wound dressing and burn dressing.
Non Electromedic Non Sterile
NETROD™ Radio Frequency Renal Ablation Catheter
SHANGHAI GOLDEN LEAF MEDTECH CO., LTD.
BONEUNION MEDICAL Upper Limb Plate
BONEUNION (XIAMEN) MEDICAL DEVICE CO., LTD.
INNOLCON Ultrasonic Surgical System
INNOLCON MEDICAL TECHNOLOGY (SUZHOU) CO., LTD. (BUILDING 10)
NETROD™ Radio Frequency Renal Ablation Device
SHANGHAI GOLDEN LEAF MEDTECH CO., LTD.
PERMEADERM Biosynthetic Wound Matrix
TRELLEBORG SEALING SOLUTIONS US, INC.
PERMEADERM Biosynthetic Wound Matrix
TRELLEBORG SEALING SOLUTIONS US, INC.
PHONAK TERRA+ RIC-312
SONOVA AT
PHONAK TERRA+ BTE-M
SONOVA AT
PHONAK TERRA BTE-M
SONOVA AT
PHONAK TERRA+ BTE-UP
SONOVA AT