VACUSERA Blood Collection Needle - Indonesia BPOM Medical Device Registration
VACUSERA Blood Collection Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902616110. The device is manufactured by DISERA MEDICAL MATERIAL LOGISTICS INDUSTRY AND TRADE CO. INC. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is HOSPI MEDIK INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Country of Origin
Turkey
Authorized Representative
HOSPI MEDIK INDONESIAAR Address
Gedung Indra Sentral Blok E-F Lantai 1-2 Jl. Letjen Suprapto No. 60 Kel. Cempaka Putih Barat Kec. Cempaka Putih, Jakarta Pusat 10520
Registration Date
Sep 20, 2024
Expiry Date
Dec 31, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Sterile
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