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ENVISION™ FLEX Antibody Diluent - Indonesia BPOM Medical Device Registration

ENVISION™ FLEX Antibody Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208817609. The device is manufactured by DAKO DENMARK APS. from Denmark, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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BPOM Registered
Risk Class Kelas Resiko : B
ENVISION™ FLEX Antibody Diluent
Analysis ID: AKL 20208817609

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

DAKO DENMARK APS.

Country of Origin

Denmark

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 1-2 Jl. Tentara Pelajar No. 5

Registration Date

Aug 16, 2020

Expiry Date

May 22, 2024

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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