SUCTION ASPIRATOR Single Pump - Indonesia BPOM Medical Device Registration

SUCTION ASPIRATOR Single Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603125313. The device is manufactured by GIMA, S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDICAL BLESSINGS OF THE ARCHIPELAGO.

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BPOM Registered

Risk Class Kelas Resiko : B

SUCTION ASPIRATOR Single Pump

Analysis ID: AKL 21603125313

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GIMA, S.P.A

Country of Origin

Italy

Authorized Representative

MEDICAL BLESSINGS OF THE ARCHIPELAGO

AR Address

JALAN RUKAN SEDAYU SQUARE BLOK K-19, CENGKARENG

Registration Date

Aug 30, 2021

Expiry Date

Dec 31, 2023

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

DJ Fang

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