Pure Global

AESCULAP Nuerosurgery Cranio Plate - Indonesia BPOM Medical Device Registration

AESCULAP Nuerosurgery Cranio Plate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003904248. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
AESCULAP Nuerosurgery Cranio Plate
Analysis ID: AKL 21003904248

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

AESCULAP AG

Country of Origin

Germany

Authorized Representative

PT. 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

Dec 15, 2022

Expiry Date

May 17, 2025

Product Type

Therapeutic Neurology Equipment

Preformed alterable cranioplasty plate.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing