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DIAGAST CleanLys - Indonesia BPOM Medical Device Registration

DIAGAST CleanLys is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10204412216. The device is manufactured by DIAGAST. from France, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDQUEST JAYA GLOBAL.

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BPOM Registered
Risk Class Kelas Resiko : A
DIAGAST CleanLys
Analysis ID: AKL 10204412216

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DIAGAST.

Country of Origin

France

Authorized Representative

PT. MEDQUEST JAYA GLOBAL

AR Address

Menara Salemba Lantai 6 Jl. Salemba Raya Kav. 5 - 5A

Registration Date

Nov 23, 2022

Expiry Date

Aug 11, 2027

Product Type

Reagents and Specimen Providers

General purpose reagent.

Invitro Diagnostics

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