GREINER BIO-ONE Standard Tube Holder - Indonesia BPOM Medical Device Registration
GREINER BIO-ONE Standard Tube Holder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902913544. The device is manufactured by GREINER BIO-ONE GMBH from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GREINER BIO-ONE GMBHCountry of Origin
Austria
Authorized Representative
PT. SABA INDOMEDIKAAR Address
Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9
Registration Date
Dec 29, 2023
Expiry Date
Jul 02, 2026
Product Type
Therapeutic General and Individual Hospital Equipment
Hypodermic single lumen needle.
Non Electromedic Non Sterile
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