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MES Lungtest Mobile Spirometer - Indonesia BPOM Medical Device Registration

MES Lungtest Mobile Spirometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401411284. The device is manufactured by MY SP. ZO. O from Poland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ASA PRATAMA PARTNERS.

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BPOM Registered
Risk Class Kelas Resiko : B
MES Lungtest Mobile Spirometer
Analysis ID: AKL 20401411284

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MY SP. ZO. O

Country of Origin

Poland

Authorized Representative

ASA PRATAMA PARTNERS

AR Address

MT Haryono Square No.OF 01/06 JL. MT.Haryono Kav.10, Kel. Bidara Cina , Kec. Jatinegara - Jakarta Timur

Registration Date

May 21, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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