IN-PORT Polymer Access Port - Indonesia BPOM Medical Device Registration
IN-PORT Polymer Access Port is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902817336. The device is manufactured by ISOMED S.A.R.L from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PELITA BIOMEDICAL.
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
ISOMED S.A.R.LCountry of Origin
France
Authorized Representative
PT. PELITA BIOMEDICALAR Address
Gedung Autobridal Lantai4 Jl. KH Abdullah Syafei No.30 Kel. Asem Baris Kec. Tebet Jakarta Selatan
Registration Date
Nov 25, 2022
Expiry Date
May 06, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Subcutaneous, implanted, intravascular infusion port and catheter.
Non Electromedic Sterile
IWIN Negative Pressure Drainage Catheter for Single-Use
JIANGSU YANGTZE RIVER MEDICAL TECHNOLOGY CORP.
SINAPI Urine Meter SUM500V2
SINAPI BIOMEDICAL PTY. LTD
SINAPI Chest Drain XL 1000S
SINAPI BIOMEDICAL PTY. LTD
EXACTA NUMBER ONE Silicone Ballon Infuser NMB
GAMASTECH SRL
SINAPI Chest Drain XL 200SC
SINAPI BIOMEDICAL CC.
SINAPI Chest Drain XL 2000SD
SINAPI BIOMEDICAL CC.
SINAPI Chest Drain XL 1000SC
SINAPI BIOMEDICAL CC.
Exacta Number One BOL
GAMASTECH SRL
ISOMED Vein Strippers
ISOMED S.A.R.L
INFU KT - Titanium Access Port Pression Injection
ISOMED S.A.R.L.