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ELEKTA Harmony Pro - Indonesia BPOM Medical Device Registration

ELEKTA Harmony Pro is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21502320106. The device is manufactured by ELEKTA BEIJING MEDICAL SYSTEMS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ELEKTA MEDICAL SOLUTIONS.

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 : C
ELEKTA Harmony Pro
Analysis ID: AKL 21502320106

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ELEKTA MEDICAL SOLUTIONS

AR Address

Cowell Tower Lantai 7 Unit 02A, Jl. Senen Raya No. 135, Kode Pos 10410, Kel. Senen, Kec. Senen, Kota Jakarta Pusat, Prov. DKI Jakarta

Registration Date

Jan 10, 2024

Expiry Date

Aug 11, 2027

Product Type

Therapeutic Radiology Equipment

Medical charged-particle radiation therapy system.

Electromedic Radiation

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