GUNA MD-KNEE H - Indonesia BPOM Medical Device Registration
GUNA MD-KNEE H is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302420309. The device is manufactured by USE S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. I-TECH LAFACOS.
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Risk Classification
Product Class
Kelas : 3
Manufacturer
USE S.P.A.Country of Origin
Italy
Authorized Representative
PT. I-TECH LAFACOSAR Address
Gedung indra centra Blok M-N, Jl. Jendral suprapto No. 60, Kel Cempaka Putih barat , Kec. Cempaka Putih
Registration Date
Aug 27, 2024
Expiry Date
May 31, 2027
Product Type
Prosthetic Orthopedic Equipment
Intra articular fluid
Non Electromedic Sterile
DISCOVERY Pico Derm
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