TITA JET™ Light II Contrast - Indonesia BPOM Medical Device Registration
TITA JET™ Light II Contrast is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322512. The device is manufactured by PFM MEDICAL CPP SA from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. NUGRA KARSERA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
PFM MEDICAL CPP SACountry of Origin
Switzerland
Authorized Representative
PT. NUGRA KARSERAAR Address
Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10
Registration Date
Sep 05, 2023
Expiry Date
May 15, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Subcutaneous, implanted, intravascular infusion port and catheter.
Non Electromedic Sterile
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