URIMED Cath All Silicone Folley Catheter Nelaton - Indonesia BPOM Medical Device Registration
URIMED Cath All Silicone Folley Catheter Nelaton is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805220156. The device is manufactured by WELL LEAD MEDICAL CO. LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. B. BRAUN 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
WELL LEAD MEDICAL CO. LTD.Country of Origin
China
Authorized Representative
PT. B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Jun 02, 2022
Expiry Date
Oct 10, 2025
Product Type
Therapeutic Gastroenterology-Urology Equipment
Urological catheter and accessories.
Non Electromedic Sterile
AESCULAP Scalpel & Knives
AESCULAP AG.
AESCULAP Multi Interchangeable Trocar System
AESCULAP AG.
AESCULAP Gynaecology Scissors
AESCULAP AG.
CYTO-SET Infusomat Plus
B. BRAUN MEDICAL KFT. PRODUCTION DIVISION
AESCULAP Saw Blades
AESCULAP AG.
AESCULAP Leyla Retractor
AESCULAP AG., GERMANY
AESCULAP Electrosurgical Endoscopy Equipment
AESCULAP AG
AESCULAP Fine Wound Retractor
AESCULAP AG.
AESCULAP Hi-Line XXS
AESCULAP AG.
AESCULAP Micro-Line and Accessories
AESCULAP AG.