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PHILIPS Avalon Fetal Monitor FM 20 - Indonesia BPOM Medical Device Registration

PHILIPS Avalon Fetal Monitor FM 20 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21102011968. The device is manufactured by PHILIPS MEDIZIN SYSTEME BOEBLINGEN GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.

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Risk Class Kelas Resiko : B
PHILIPS Avalon Fetal Monitor FM 20
Analysis ID: AKL 21102011968

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PHILIPS INDONESIA COMMERCIAL

AR Address

Gedung Cibis Nine Lantai 10, Jl. TB Simatupang No. 2

Registration Date

Mar 17, 2022

Expiry Date

Aug 25, 2026

Product Type

Obstetric and Gynecological Monitoring Equipment

Fetal cardiac monitor.

Non Radiation Electromedics

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