SPACER-K - Indonesia BPOM Medical Device Registration
SPACER-K is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302612282. The device is manufactured by TECRES S.P.A. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENDO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TECRES S.P.A.Country of Origin
Italy
Authorized Representative
PT. ENDO INDONESIAAR Address
Jl. Raya Menganti 14
Registration Date
Apr 30, 2022
Expiry Date
Dec 31, 2026
Product Type
Prosthetic Orthopedic Equipment
Knee joint femorotibial metal/polymer semi-constrained cemented prosthesis.
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