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INVIDIA ESU-IM-400 - Indonesia BPOM Medical Device Registration

INVIDIA ESU-IM-400 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520017. The device is manufactured by ENVY MEDICAL GMBH & CO., KG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. CITRA DIAN PRATAMA.

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
INVIDIA ESU-IM-400
Analysis ID: AKL 21603520017

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. CITRA DIAN PRATAMA

AR Address

Jalan Panjang No. 38

Registration Date

Jan 03, 2025

Expiry Date

Dec 31, 2026

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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