MINICOLLECT TUBE K2E K2EDTA - Indonesia BPOM Medical Device Registration
MINICOLLECT TUBE K2E K2EDTA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101915403. 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 SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 2
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
Mar 28, 2024
Expiry Date
Jul 02, 2026
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
VACUETTE Blood Culture Holder
VACUETTE TUBE CAT Serum Fast Separator
VACUETTE QUICKSHIELD Safety Tube Holder
VACUETTE SECONDARY Tube MULTIPLEX PP
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VACUETTE LH Lithium Heparin Separator
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VACUETTE TUBE FX Sodium Fluoride / Potassium Oxalate
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VACUETTE TUBE CAT Serum Fast Separator
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VACUETTE Luer Adapter
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VACUETTE SECONDARY Tube MULTIPLEX PP
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VACUETTE Tube CPDA
GREINER BIO-ONE GMBH.