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DIXION Dual Syringe Pump - Indonesia BPOM Medical Device Registration

DIXION Dual Syringe Pump is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902125543. The device is manufactured by DIXION VERTRIEB MEDIZINISCHER GERร„TE GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDIKA INDO BAVARIA.

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
DIXION Dual Syringe Pump
Analysis ID: AKL 20902125543

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. MEDIKA INDO BAVARIA

AR Address

Ruko Green Garden Blok A 14 No. 10 RT. 05 / RW. 03

Registration Date

Feb 20, 2022

Expiry Date

Sep 10, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Infusion pump.

Non Radiation Electromedics

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