LIND-VAC® EDTA K2 Vacuum Blood Collection Tubes - Indonesia BPOM Medical Device Registration
LIND-VAC® EDTA K2 Vacuum Blood Collection Tubes is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101912984. The device is manufactured by INTERVACTECHNOLOGY OR. from Estonia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. Rajawali Nusindo.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
INTERVACTECHNOLOGY OR.Country of Origin
Estonia
Authorized Representative
PT. Rajawali NusindoAR Address
Gedung RNI Jl. Denpasar Raya Kav DIII Kuningan Jakarta Selatan
Registration Date
May 13, 2019
Expiry Date
Dec 11, 2023
Product Type
Clinical Chemistry Test System
Blood specimen collection device
Invitro Diagnostics
DGM ANDS Steam Sterilizer
PROHS S.A
DGM ANDS Steam Sterilizer
PROHS S.A
DGM ANDS Steam Sterilizer
PROHS S.A
DGM ANDS Steam Sterilizer
PROHS S.A
DGM ANDS Steam Sterilizer
PROHS S.A
DGM ANDS Steam Sterilizer
PROHS S.A

