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RAR Flexi Probe - Indonesia BPOM Medical Device Registration

RAR Flexi Probe is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501313680. The device is manufactured by A.M.I. AGENCY FOR MEDICAL INNOVATIONS GMBH from Austria, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is DIAN LANGGENG PRATAMA.

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BPOM Registered
Risk Class Kelas Resiko : B
RAR Flexi Probe
Analysis ID: AKL 21501313680

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Austria

Authorized Representative

DIAN LANGGENG PRATAMA

AR Address

Gedung Dinar, Jl. Raden Saleh Raya No. 4 RT.10/RW.01, Kel. Kenari, Kec. Senen. Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos 10430

Registration Date

May 10, 2023

Expiry Date

Dec 31, 2026

Product Type

Diagnostic Radiology Equipment

Diagnostic ultrasonic transducer.

Non Electromedic Sterile

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