UROMEDTECH UROMASTER® ADVENTURE - Indonesia BPOM Medical Device Registration
UROMEDTECH UROMASTER® ADVENTURE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420800. The device is manufactured by UROMEDTECH PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ANDAMAN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
UROMEDTECH PTE LTDCountry of Origin
Singapore
Authorized Representative
PT. ANDAMAN MEDICAL INDONESIAAR Address
Menara Cardig Lantai 1, Jalan Raya Halim Perdanakusuma
Registration Date
Nov 14, 2024
Expiry Date
Aug 29, 2029
Product Type
Diagnostic Radiology Equipment
Ultrasonic pulsed doppler imaging system.
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