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KANGHUI Implant -Trauma - Indonesia BPOM Medical Device Registration

KANGHUI Implant -Trauma is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302714344. The device is manufactured by CHANGZHOU KANGHUI MEDICAL INNOVATION CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MEDTRONIC INDONESIA.

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BPOM Registered
Risk Class Kelas Resiko : C
KANGHUI Implant -Trauma
Analysis ID: AKL 21302714344

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. MEDTRONIC INDONESIA

AR Address

Gandaria 8 Office Tower Lantai 36 Unit A, Jl. Sultan Iskandar Muda

Registration Date

Sep 18, 2022

Expiry Date

Jan 13, 2026

Product Type

Prosthetic Orthopedic Equipment

Single/multiple component metallic bone fixation appliances and accessories.

Non Electromedic Non Sterile

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