ARROWBONE-B - Indonesia BPOM Medical Device Registration
ARROWBONE-B is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20602027460. The device is manufactured by BRAINBASE CORPORATION, TOKYO FACTORY from Japan, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. WOORI BIO CORPORA.
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.
ARROWBONE-ฮฒ
Risk Classification
Product Class
Kelas : 2
Manufacturer
BRAINBASE CORPORATION, TOKYO FACTORYCountry of Origin
Japan
Authorized Representative
PT. WOORI BIO CORPORAAR Address
KOMPLEK GOLDEN PLAZA FATMAWATI BLOK E-43, JL. RS FATMAWATI NO. 15, JAKARTA SELATAN, DKI JAKARTA 12420
Registration Date
Dec 01, 2020
Expiry Date
Sep 04, 2025
Product Type
Prosthetic Dental Equipment
Bone grafting material.
Non Electromedic Sterile
PRIME Latex Examination Glove Powder Free
APEX MEDISOURCE SDN., BHD.
PRIME Latex Examination Glove Powdered
APEX MEDISOURCE SDN., BHD.
INTELLIS LUCENXIA Automated Peritoneal Dialysis System
YUSOFF ENGINEERING SDN BHD.
CONNECX Sofpad Alcohol Swab
SUN HEALTHCARE (M) SDN. BHD.
CONNECX Uronecx Latex Foley Catheter 3 Way
WELL LEAD MEDICAL CO., LTD.
CONNECX Uronecx Latex Foley Catheter 2 Way
WELL LEAD MEDICAL CO., LTD.
CONNECX Respinecx Endotracheal Tube Cuffed
WELL LEAD MEDICAL CO., LTD.
ARROW FIT-System
BRAINBASE CORPORATION, TOKYO FACTORY, KOSEN-SHA THE 2ND FACTORY
MYTIS Attachment Caps
BRAINBASE CORPORATION, TOKYO FACTORY
Arrow Implant
BRAINBASE CORPORATION

