PAVIS Compression Ankle - Indonesia BPOM Medical Device Registration
PAVIS Compression Ankle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11402714811. The device is manufactured by PAVIS S.P.A. from Italy, 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
PAVIS S.P.A.Country of Origin
Italy
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
May 28, 2021
Expiry Date
Jan 20, 2026
Product Type
Prosthetic Physical Health Equipment
Limb orthosis.
Non Electromedic Non Sterile
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