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DIMEDA Herniotomy Set - Indonesia BPOM Medical Device Registration

DIMEDA Herniotomy Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603712362. The device is manufactured by DIMEDA TOOLS GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ERA SURYA PERSADA.

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 : A
DIMEDA Herniotomy Set
Analysis ID: AKL 11603712362

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

DIMEDA TOOLS GMBH

Country of Origin

Germany

Authorized Representative

PT. ERA SURYA PERSADA

AR Address

Graha Mas Pemuda Blok AD 12 Jl. Pemuda Rawamngun, Jakarta

Registration Date

Dec 07, 2020

Expiry Date

Jul 28, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Sterile

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