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IVIS PRECISIO HX001 - Indonesia BPOM Medical Device Registration

IVIS PRECISIO HX001 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21201220162. The device is manufactured by IVIS TECHNOLOGIES S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HARLISA TRUE GRACE.

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BPOM Registered
Risk Class Kelas Resiko : B
IVIS PRECISIO HX001
Analysis ID: AKL 21201220162

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PT. HARLISA TRUE GRACE

AR Address

Jalan Sriti Blok HH-15, Perumahan Sedati Permai

Registration Date

Sep 25, 2022

Expiry Date

Dec 31, 2027

Product Type

Diagnostic Eye Equipment

Optical Coherence Tomography

Non Radiation Electromedics

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