ERYCARD 2.0 - Indonesia BPOM Medical Device Registration
ERYCARD 2.0 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20209320505. The device is manufactured by TULIP DIAGNOSTICS (P) LTD from India, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is GRAVIA CITRA LESTARI.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
TULIP DIAGNOSTICS (P) LTDCountry of Origin
India
Authorized Representative
GRAVIA CITRA LESTARIAR Address
Komplek Rukan Gading Bukit Indah Blok C15 Jl. Bukit Gading Raya
Registration Date
Jun 07, 2023
Expiry Date
Nov 23, 2027
Product Type
Products used in the manufacture of blood preparations and preparations of origin and blood
Automated blood grouping and antibody test system.
Invitro Diagnostics
