SURU Ureteral Stent Kit (Double J Stent) - Indonesia BPOM Medical Device Registration
SURU Ureteral Stent Kit (Double J Stent) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804910726. The device is manufactured by SURU INTERNATIONAL PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SUCCESS WITH DAVID.
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
SURU INTERNATIONAL PVT. LTD.Country of Origin
India
Authorized Representative
PT. SUCCESS WITH DAVIDAR Address
GEDUNG NUCIRA LANTAI 3 JL. MT. HARYONO KAV. 27 KEL. TEBET TIMUR
Registration Date
Feb 15, 2019
Expiry Date
Dec 31, 2023
Product Type
Gastroenterology-Surgical Urology Equipment
Ureteral stent.
Non Electromedic Sterile
HYSONIC YACHT
JLU CO., LTD
NAZIR & HABIB Forceps
Nazir & Habib Corporation
MEDIPIA NK Light
MEDIPIA CO., LTD
Nazir & Habib Fui Punch
Nazir & Habib Corporation
NK Magnifier
MEDIPIA CO., LTD
MCURE AQUAPEN2
MCURE CO., LTD.
MINERVA PDO Suture
CNG CO., LTD.
DR. CANNULA
YONG CHANG CO.,LTD
INSTAR S1 with Lidocaine
BIOPLUS CO., LTD
INSTAR S2 with Lidocaine
BIOPLUS CO., LTD

