APTOS Nano Vitis Method - Indonesia BPOM Medical Device Registration
APTOS Nano Vitis Method is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603817707. The device is manufactured by FEUERSTEIN GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is 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
FEUERSTEIN GMBHCountry of Origin
Germany
Authorized Representative
ETERNAL VAST OCEANAR Address
Jl. Tanah Abang IV No. 34B, RT 004 / RW 03, Gambir, Jakarta Pusat
Registration Date
Dec 23, 2022
Expiry Date
Dec 31, 2024
Product Type
Surgical Equipment
Absorbable poly(glycolide/ l -lactide) surgical suture.
Non Electromedic Sterile
APTOS Light Lift Thread Method Blunt
APTOS Excellence Visage Method HA
APTOS Light Lift Thread Method
APTOS Light Lift Needle Method S
APTOS Nano Excellence Method
APTOS Visage Excellence Method
APTOS Light Lift Linea Method
APTOS Nano Spring Method
APTOS Sole Rhinoplasty Method
APTOS Light Lift Needle Method B
APTOS Visage Excellence Method S HA
APTOS LLC
MIRROR CANNULA Filler & Fat Graft Cannula
NANUM COMPANY CO, LTD
APTOS Light Lift Thread Method Blunt
FEUERSTEIN GMBH
APTOS Excellence Visage Method HA
FEUERSTEIN GMBH
APTOS Light Lift Needle Method S
FEUERSTEIN GMBH
APTOS Visage Excellence Method
FEUERSTEIN GMBH

