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AESCULAP Art(h)cut - Indonesia BPOM Medical Device Registration

AESCULAP Art(h)cut is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11303610486. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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
AESCULAP Art(h)cut
Analysis ID: AKL 11303610486

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

AESCULAP AG

Country of Origin

Germany

Authorized Representative

B. BRAUN MEDICAL INDONESIA

AR Address

Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan

Registration Date

Oct 17, 2022

Expiry Date

May 17, 2025

Product Type

Surgical Orthopaedic Equipment

Orthopedic manual surgical instrument.

Non Electromedic Sterile

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