OMNIFIX Single Use Syringe without Needle - Indonesia BPOM Medical Device Registration
OMNIFIX Single Use Syringe without Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902600242. The device is manufactured by ALMO ERZEUGNISSE ERWIN BUSCH GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
ALMO ERZEUGNISSE ERWIN BUSCH GMBHCountry of Origin
Germany
Authorized Representative
B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Dec 12, 2022
Expiry Date
Jan 12, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Piston syringe.
Non Electromedic Sterile
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