MYSELLA CARE Bed Type KY302D-32 - Indonesia BPOM Medical Device Registration
MYSELLA CARE Bed Type KY302D-32 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902513961. The device is manufactured by GUANGDONG KAIYANG MEDICAL TECHNOLOGY GROUP 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 23, 2020
Expiry Date
Mar 03, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
AC-powered adjustable hospital bed.
Non Electromedic Non Sterile
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