ROSA Knee Instrument - Indonesia BPOM Medical Device Registration
ROSA Knee Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320356. The device is manufactured by ZIMMER CAS from Canada, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is KALMED SEJAHTERA INDONESIA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
ZIMMER CASCountry of Origin
Canada
Authorized Representative
KALMED SEJAHTERA INDONESIAAR Address
Jl. TMII Pintu II No. 2, RT 006 RW 004,
Registration Date
Mar 30, 2023
Expiry Date
Dec 08, 2026
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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