Pure Global

ALCARE Multi Fix - Indonesia BPOM Medical Device Registration

ALCARE Multi Fix is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902420461. The device is manufactured by ALCARE CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SEKARGUNA 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
ALCARE Multi Fix
Analysis ID: AKL 10902420461

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ALCARE CO., LTD.

Country of Origin

Japan

Authorized Representative

SEKARGUNA MEDIKA

AR Address

JL. Ciputat Raya Nomor 64

Registration Date

May 07, 2024

Expiry Date

May 30, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Medical adhesive tape and adhesive bandage, non sterile

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing