SELLA Alternating Pressure/Bubble Mattress - Indonesia BPOM Medical Device Registration
SELLA Alternating Pressure/Bubble Mattress is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902715703. The device is manufactured by GUANGDONG YUEHUA MEDICAL INSTRUMENT FACTORY CO LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DAYA AGUNG MANDIRI.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
China
Authorized Representative
PT. DAYA AGUNG MANDIRIAR Address
JL S. HASANUDIN NO 23 PERUM POLEKO RT 001/001 DESA TAMBUN KEC TAMBUN SELATAN
Registration Date
Apr 27, 2022
Expiry Date
May 13, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Alternating pressure air flotation mattress.
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