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LUXAMED LuxaScope Sonus Adult Flex Stethoscope - Indonesia BPOM Medical Device Registration

LUXAMED LuxaScope Sonus Adult Flex Stethoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10501610318. The device is manufactured by LUXAMED GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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BPOM Registered
Risk Class Kelas Resiko : A
LUXAMED LuxaScope Sonus Adult Flex Stethoscope
Analysis ID: AKL 10501610318

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Apr 27, 2022

Expiry Date

May 09, 2027

Product Type

Diagnostic Cardiology Equipment

Stethoscope.

Non Electromedic Non Sterile

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