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KOEL TRINITY - Indonesia BPOM Medical Device Registration

KOEL TRINITY is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501321393. The device is manufactured by KOELIS from France, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TRANSMEDIC INDONESIA.

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Risk Class Kelas Resiko : B
KOEL TRINITY

KOELIS TRINITY

Analysis ID: AKL 21501321393

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

KOELIS

Country of Origin

France

Authorized Representative

TRANSMEDIC INDONESIA

AR Address

PERKANTORAN MENARA ERA UNIT G-01, JL. SENEN RAYA NO. 135-137

Registration Date

Nov 21, 2023

Expiry Date

Apr 21, 2028

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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