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KMER Hematology Reagent - Diluent - Indonesia BPOM Medical Device Registration

KMER Hematology Reagent - Diluent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208220307. The device is manufactured by WHEISMAN MEDICAL TECHNOLOGY CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INDOPHARM NUSANTARA BIOMEDICINE.

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BPOM Registered
Risk Class Kelas Resiko : B
KMER Hematology Reagent - Diluent
Analysis ID: AKL 20208220307

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. INDOPHARM NUSANTARA BIOMEDICINE

AR Address

Jalan Griya Agung Blok O No.72,

Registration Date

Oct 22, 2022

Expiry Date

Jun 29, 2027

Product Type

Hematological Reagents

Blood cell diluents

Invitro Diagnostics

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