RIGIDLOOP Instrument - Indonesia BPOM Medical Device Registration
RIGIDLOOP Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303320423. The device is manufactured by MEDOS SARL. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. JOHNSON AND JOHNSON INDONESIA TWO.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDOS SARL.Country of Origin
Switzerland
Authorized Representative
PT. JOHNSON AND JOHNSON INDONESIA TWOAR Address
K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950
Registration Date
Jun 16, 2023
Expiry Date
Feb 21, 2028
Product Type
Surgical Orthopaedic Equipment
Orthopedic manual surgical instrument.
Non Electromedic Non Sterile
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