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GIDCARE Case Sterile - Indonesia BPOM Medical Device Registration

GIDCARE Case Sterile is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902023060. The device is manufactured by NANTONG HOPE INDUSTRY & TRADE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is GIDION JAYA.

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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Risk Class Kelas Resiko : A
GIDCARE Case Sterile

GIDCARE Kasa Steril

Analysis ID: AKL 10902023060

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

GIDION JAYA

AR Address

JL SULTAN HASANUDIN RT 005 / RW 05, AMBON 97128, MALUKU

Registration Date

May 29, 2023

Expiry Date

Dec 31, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Nonresorbable gauze/sponge for external use, sterile

Non Electromedic Sterile

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