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DORNIER DELTA III Pro (XRAY 15KW/SW E180) - Indonesia BPOM Medical Device Registration

DORNIER DELTA III Pro (XRAY 15KW/SW E180) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20805320569. The device is manufactured by DORNIER MEDTECH SYSTEMS GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.

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
DORNIER DELTA III Pro (XRAY 15KW/SW E180)
Analysis ID: AKL 20805320569

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. PERMANA PUTRA MANDIRI

AR Address

Taman Mini Pintu II Atas No.9 Jakarta Timur

Registration Date

Feb 02, 2023

Expiry Date

May 12, 2027

Product Type

Therapeutic Gastroenterology-Urology Equipment

Extracorporeal shock wave lithotripter.

Electromedic Radiation

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