VACUETTE SECONDARY Tube MULTIPLEX PP - Indonesia BPOM Medical Device Registration
VACUETTE SECONDARY Tube MULTIPLEX PP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10203916354. The device is manufactured by GREINER BIO-ONE GMBH from Austria, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
GREINER BIO-ONE GMBHCountry of Origin
Austria
Authorized Representative
SABA INDOMEDIKAAR Address
Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9
Registration Date
Apr 29, 2024
Expiry Date
Jul 02, 2026
Product Type
Pathology Equipment and Accessories
Specimen transport and storage container.
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