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ALCARE Procare MF Pate - Indonesia BPOM Medical Device Registration

ALCARE Procare MF Pate is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10805127316. 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 PT. 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.

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BPOM Registered
Risk Class Kelas Resiko : A
ALCARE Procare MF Pate
Analysis ID: AKL 10805127316

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

ALCARE CO., LTD.

Country of Origin

Japan

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

jl.Ciputat Raya no 14 B.Pondok Pinang

Registration Date

Nov 27, 2021

Expiry Date

May 09, 2025

Product Type

Therapeutic Gastroenterology-Urology Equipment

Ostomy pouch and accessories.

Non Electromedic Non Sterile

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