QUIKLYTE Integrated Multisensor Sample Diluent. - Indonesia BPOM Medical Device Registration

QUIKLYTE Integrated Multisensor Sample Diluent. is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208122132. The device is manufactured by NOVA BIOMEDICAL CORPORATION. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SIEMENS HEALTHINEERS INDONESIA.

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BPOM Registered

Risk Class Kelas Resiko : B

QUIKLYTE Integrated Multisensor Sample Diluent.

Analysis ID: AKL 20208122132

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NOVA BIOMEDICAL CORPORATION.

Country of Origin

United States

Authorized Representative

SIEMENS HEALTHINEERS INDONESIA

AR Address

Perkantoran Hijau Arkadia Tower F, Lantai 18, Jl.Tahi Bonar Simatupang Kav. 88

Registration Date

Feb 06, 2025

Expiry Date

Aug 01, 2029

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

DJ Fang

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Other Products from NOVA BIOMEDICAL CORPORATION.

Products from the same manufacturer (10 products)

QUIKLYTE Integrated Multisensor Sample Diluent. - Indonesia BPOM Medical Device Registration

Risk Classification

Product Class

Manufacturer

Country of Origin

Authorized Representative

AR Address

Registration Date

Expiry Date

Product Type

DJ Fang

QUIKLYTE Integrated Multisensor Standard A

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