PRIME Latex Examination Glove Powdered - Indonesia BPOM Medical Device Registration
PRIME Latex Examination Glove Powdered is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10903220937. The device is manufactured by APEX MEDISOURCE SDN., BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : A. 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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
APEX MEDISOURCE SDN., BHD.Country of Origin
Malaysia
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
Aug 12, 2022
Expiry Date
Feb 14, 2027
Product Type
General Hospital Equipment and Other Individuals
Patient examination glove.
Non Electromedic Non Sterile
PRIME Latex Examination Glove Powder Free
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
ARROWBONE-B
BRAINBASE CORPORATION, TOKYO FACTORY
Arrow Implant
BRAINBASE CORPORATION