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AGAPPE ASO mispa i3 - Indonesia BPOM Medical Device Registration

AGAPPE ASO mispa i3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10303719153. The device is manufactured by AGAPPE DIAGNOSTICS SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is MULTIMEDILAB KARYAMANDIRI.

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BPOM Registered
Risk Class Kelas Resiko : C
AGAPPE ASO mispa i3
Analysis ID: AKL 10303719153

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

MULTIMEDILAB KARYAMANDIRI

AR Address

GP plaza lantai 3 unit 6, jalan Gelora II No. 01

Registration Date

Jun 21, 2022

Expiry Date

Feb 07, 2027

Product Type

Serological Reagents

Streptococcus spp. serological reagents.

Invitro Diagnostics

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