TSK STERIJECT Premium Disposable Hypodermic Needle - Indonesia BPOM Medical Device Registration
TSK STERIJECT Premium Disposable Hypodermic Needle is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902810298. The device is manufactured by TSK LABORATORY, JAPAN SOJA NO. 1 FACTORY from Japan, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TSK LABORATORY, JAPAN SOJA NO. 1 FACTORYCountry of Origin
Japan
Authorized Representative
PT. REGENESIS INDONESIAAR Address
Jl. Sultan Iskandar Muda No. 7A & B
Registration Date
Sep 21, 2022
Expiry Date
Jun 15, 2027
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
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