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VacuDAP (Dose Area Product Measuring System) - Indonesia BPOM Medical Device Registration

VacuDAP (Dose Area Product Measuring System) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21501420557. The device is manufactured by VACUTEC ME [BETA] TECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is YOSINDO MEDICAL VISION.

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
VacuDAP (Dose Area Product Measuring System)
Analysis ID: AKL 21501420557

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

YOSINDO MEDICAL VISION

AR Address

JALAN INPRES NOMOR : 268. D.

Registration Date

Aug 26, 2024

Expiry Date

Dec 31, 2028

Product Type

Diagnostic Radiology Equipment

Implanted ionizing radiation dosimeter

Non Radiation Electromedics

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