STRYKER Arthroscopy Manual Instrument Set - Indonesia BPOM Medical Device Registration
STRYKER Arthroscopy Manual Instrument Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21301910149. The device is manufactured by STRYKER ENDOSCOPY. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSMEDIC INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
STRYKER ENDOSCOPY.Country of Origin
United States
Authorized Representative
PT. TRANSMEDIC INDONESIAAR Address
Perkantoran Menara Era Unit G-01 JL.Senen Raya No.135-137 RT 00 RW 00, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Senen, Kel. Senen
Registration Date
Jul 12, 2024
Expiry Date
Feb 09, 2028
Product Type
Diagnostic Orthopedic Equipment
Arthroscope
Non Electromedic Non Sterile
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