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ANSPACH eG1 High Speed System - Indonesia BPOM Medical Device Registration

ANSPACH eG1 High Speed System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002320141. The device is manufactured by THE ANSPACH EFFORT INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is JOHNSON AND JOHNSON INDONESIA TWO.

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
ANSPACH eG1 High Speed System
Analysis ID: AKL 21002320141

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

JOHNSON AND JOHNSON INDONESIA TWO

AR Address

K-Link Tower, Lt. 15, Jl. Jend. Gatot Subroto kav. 59A, Kuningan, Setiabudi, Jakarta Selatan, Desa/Kelurahan Kuningan Timur, Kec. Setiabudi, Kota Adm. Jakarta Selatan, Provinsi DKI Jakarta, Kode Pos: 12950

Registration Date

May 29, 2023

Expiry Date

Jan 10, 2028

Product Type

Surgical Neurology Equipment

Electric cranial drill motor.

Non Radiation Electromedics

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