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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.

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BPOM Registered
Risk Class Kelas Resiko : C
CANWELL Spinal Fixation Device
Analysis ID: AKL 21302321062

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

GREENS SURGIKA INDOTAMA

AR 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

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