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CHUNLI CF Posterior Spinal Fixation Device - Indonesia BPOM Medical Device Registration

CHUNLI CF Posterior Spinal Fixation Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302320768. The device is manufactured by BEIJING CHUNLIZHENGDA MEDICAL INSTRUMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ASIA ACTUAL INDONESIA.

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Risk Class Kelas Resiko : C
CHUNLI CF Posterior Spinal Fixation Device
Analysis ID: AKL 21302320768

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ASIA ACTUAL INDONESIA

AR Address

PERKANTORAN GANDARIA 8 LANTAI 6 UNIT JL. SULTAN ISKANDAR MUDA KEBAYORAN LAMA UTARA JAKARTA SELATAN

Registration Date

Jul 11, 2023

Expiry Date

Mar 14, 2028

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Non Sterile

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