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AIMTECH Forceps Instrument 2 - Indonesia BPOM Medical Device Registration

AIMTECH Forceps Instrument 2 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603222741. The device is manufactured by AMNOTEC INTERNATIONAL MEDICAL GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is ARMICO CORE MEDIKA.

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
AIMTECH Forceps Instrument 2
Analysis ID: AKL 11603222741

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

ARMICO CORE MEDIKA

AR Address

Jl. Bedugul 1A No. 3

Registration Date

Nov 17, 2022

Expiry Date

Nov 16, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use

Non Electromedic Non Sterile

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