APTOS Body Wire Method 3/0 - Indonesia BPOM Medical Device Registration
APTOS Body Wire Method 3/0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603420133. The device is manufactured by APTOS LLC from Georgia, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ETERNAL VAST OCEAN.
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
APTOS LLCCountry of Origin
Georgia
Authorized Representative
PT. ETERNAL VAST OCEANAR Address
JALAN TANAH ABANG IV NO. 34B
Registration Date
Jan 16, 2024
Expiry Date
Nov 10, 2025
Product Type
Surgical Equipment
Stainless steel suture.
Non Electromedic Sterile
APTOS Intimate Excellence Method
APTOS Visage Excellence Method S HA
APTOS Visage Excellence Method HA
APTOS Body Excellence Method
APTOS Intimate Excellence Method HA
APTOS Light Lift Spring Method Soft
LIGHT LIFT Spring Method
APTOS Intimate Excellence Method
APTOS LLC
APTOS Visage Excellence Method HA
APTOS LLC
APTOS Body Wire Method 2/0
APTOS LLC.
AIRMESO SCALP
MCURE., CO., LTD
APTOS Body Excellence Method
APTOS LLC
APTOS Intimate Excellence Method HA
APTOS LLC
VIRTUE RF
SHENB CO., LTD.
PLURYAL Silk
MD SKIN SOLUTIONS
PLURYAL Densify
MD SKIN SOLUTIONS
APTOS Light Lift Thread Method
FEUERSTEIN GMBH

