CANWELL Spinal Fixation Device - Indonesia BPOM Medical Device Registration
CANWELL Spinal Fixation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302321062. The device is manufactured by CANWELL MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GREENS SURGIKA INDOTAMA.
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
CANWELL MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
GREENS SURGIKA INDOTAMAAR Address
GREENS SURGIKA INDOTAMA
Registration Date
Dec 19, 2023
Expiry Date
Aug 31, 2028
Product Type
Prosthetic Orthopedic Equipment
Intervertebral body fusion device
Non Electromedic Sterile

