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FISIOLINE Radiofrequency Instrument for Diathermy Therapy - Indonesia BPOM Medical Device Registration

FISIOLINE Radiofrequency Instrument for Diathermy Therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421509. The device is manufactured by FISIOLINE S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.

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Risk Class Kelas Resiko : C
FISIOLINE Radiofrequency Instrument for Diathermy Therapy
Analysis ID: AKL 21603421509

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

FISIOLINE S.R.L.

Country of Origin

Italy

Authorized Representative

PT. HARLISA TRUE GRACE

AR Address

Jalan Sriti Blok HH-15, Perumahan Sedati Permai

Registration Date

Jul 11, 2024

Expiry Date

Feb 04, 2025

Product Type

Surgical Equipment

Laser surgical instrument for use in general and plastic surgery and in dermatology.

Non Radiation Electromedics

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