ROUSEMED Post Mortem Set - Indonesia BPOM Medical Device Registration
ROUSEMED Post Mortem Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422299. The device is manufactured by ROUSEMED from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. INNOVATION HEALTHCARE INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ROUSEMEDCountry of Origin
Pakistan
Authorized Representative
PT. INNOVATION HEALTHCARE INDONESIAAR Address
Komplek Ruko Permata Kota, Blok Q No. 11 Jl. Pangeran Tubagus Angke No. 170 Kel. Penjagalan, Kec. Penjaringan, Jakarta Utara 14450
Registration Date
Oct 01, 2024
Expiry Date
Jan 01, 2028
Product Type
Surgical Equipment
Manual surgical instrument for general use
Non Electromedic Non Sterile
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