JOLINE Triple Lumen ST - Indonesia BPOM Medical Device Registration
JOLINE Triple Lumen ST is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805420027. The device is manufactured by JOLINE GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DIAN LANGGENG PRATAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
JOLINE GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
PT. DIAN LANGGENG PRATAMAAR Address
Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430
Registration Date
Jan 15, 2024
Expiry Date
Jul 06, 2026
Product Type
Therapeutic Gastroenterology-Urology Equipment
Blood access device and accessories.
Non Electromedic Sterile
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