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LITEMED ESWL LM-9200 ELMA - Indonesia BPOM Medical Device Registration

LITEMED ESWL LM-9200 ELMA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420298. The device is manufactured by LITE-MED INC. from Taiwan (China), and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NATIONAL HARMONY OF INDONESIAN TECHNOLOGY.

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Risk Class Kelas Resiko : C
LITEMED ESWL LM-9200 ELMA
Analysis ID: AKL 20805420298

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

LITE-MED INC.

Country of Origin

Taiwan (China)

AR Address

Ruko Rich Palace, No.36-40 Blok D5, Jl. Meruya Ilir, Srengseng, Kembangan, Jakarta Barat

Registration Date

Jun 06, 2024

Expiry Date

May 16, 2028

Product Type

Therapeutic Gastroenterology-Urology Equipment

Extracorporeal shock wave lithotripter.

Electromedic Radiation

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