CANWELL Lateral Lumbar Interbody Fusion System CanPEEK-L Instrument Set - Indonesia BPOM Medical Device Registration
CANWELL Lateral Lumbar Interbody Fusion System CanPEEK-L Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303420212. The device is manufactured by CANWELL MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. 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 : 1
Manufacturer
CANWELL MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
PT. GREENS SURGIKA INDOTAMAAR Address
GREENS SURGIKA INDOTAMA
Registration Date
Jul 08, 2024
Expiry Date
Aug 31, 2028
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
