CURAFIX I.V Control - Indonesia BPOM Medical Device Registration
CURAFIX I.V Control is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902124452. The device is manufactured by LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. NUSA ASIA MEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
LOHMANN & RAUSCHER INTERNATIONAL GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
PT. NUSA ASIA MEDIKAAR Address
Rukan CBD, Green Lake City F No. 15 Ketapang. Cipondoh
Registration Date
Jul 25, 2021
Expiry Date
Mar 01, 2025
Product Type
Therapeutic General and Individual Hospital Equipment
Intravascular catheter securement device.
Non Electromedic Sterile
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