CANWELL MEDICAL Transforminal Lumbar Interbody Fusion System CanPEEK-T - Indonesia BPOM Medical Device Registration
CANWELL MEDICAL Transforminal Lumbar Interbody Fusion System CanPEEK-T is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303220279. 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 FIXA MEDIKA TAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
CANWELL MEDICAL CO., LTD.Country of Origin
China
Authorized Representative
FIXA MEDIKA TAMAAR Address
RUKAN ROSES GARDEN 5, BLOK RRG N0. 50, GRAND GALAXY CITY
Registration Date
Nov 24, 2022
Expiry Date
May 01, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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