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CA-MI NEW ASKIR 20 Suction Unit - Indonesia BPOM Medical Device Registration

CA-MI NEW ASKIR 20 Suction Unit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603212974. The device is manufactured by CA-MI S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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Risk Class Kelas Resiko : B
CA-MI NEW ASKIR 20 Suction Unit
Analysis ID: AKL 21603212974

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

CA-MI S.R.L.

Country of Origin

Italy

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

May 31, 2022

Expiry Date

Apr 01, 2027

Product Type

Surgical Equipment

Powered suction pump.

Non Radiation Electromedics

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