TERUMO K-PACK II Needle - Indonesia BPOM Medical Device Registration
TERUMO K-PACK II Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902510655. The device is manufactured by TERUMO EUROPE N.V. from Belgium, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TERUMO INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TERUMO EUROPE N.V.Country of Origin
Belgium
Authorized Representative
PT. TERUMO INDONESIAAR Address
Wisma Keiai Lt.5 Jl. Jend.Sudirman Kav.3 Jakarta
Registration Date
Jan 24, 2024
Expiry Date
Feb 21, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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