SYNOLIS VA 40/80 - Indonesia BPOM Medical Device Registration
SYNOLIS VA 40/80 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302122440. The device is manufactured by APTISSEN Ltd from Switzerland, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
APTISSEN LtdCountry of Origin
Switzerland
Authorized Representative
I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
May 17, 2021
Expiry Date
Jun 25, 2025
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile

