POLYMED Huber Infusion Set - Indonesia BPOM Medical Device Registration
POLYMED Huber Infusion Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902322813. The device is manufactured by POLY MEDICURE LIMITED from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. BISAWI GROWS IN HARMONY.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
POLY MEDICURE LIMITEDCountry of Origin
India
Authorized Representative
PT. BISAWI GROWS IN HARMONYAR Address
Graha Kencana Blok EU Jl. Raya Perjuangan No.88 Kebun Jeruk Jakarta Barat
Registration Date
Aug 26, 2024
Expiry Date
Feb 15, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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