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VIVID S60N - Indonesia BPOM Medical Device Registration

VIVID S60N is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501320754. The device is manufactured by GE VINGMED ULTRASOUND AS from Norway, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GE OPERATIONS INDONESIA.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : B
VIVID S60N
Analysis ID: AKL 21501320754

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Norway

Authorized Representative

GE OPERATIONS INDONESIA

AR Address

South Quarter Tower B, Lantai 18-19 Jl. R.A. Kartini, Kav. 8 Kel. Cilandak Barat, Kec. Cilandak Jakarta Selataran 12430

Registration Date

Feb 01, 2023

Expiry Date

Oct 17, 2027

Product Type

Diagnostic Radiology Equipment

Ultrasonic pulsed doppler imaging system.

Non Radiation Electromedics

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