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KESYS Disposable Breathing Filter - Indonesia BPOM Medical Device Registration

KESYS Disposable Breathing Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403520008. The device is manufactured by SHAOXING UNDIS MEDICAL TECHNOLOGY CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ANANDA BERKAH ABADI.

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 : B
KESYS Disposable Breathing Filter
Analysis ID: AKL 20403520008

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ANANDA BERKAH ABADI

AR Address

Perumahan Duta Kranji Jalan Manyar Nomor 661 C, Desa/Kelurahan Kranji, Kec. Bekasi Barat, Kota Bekasi, Provinsi Jawa Barat

Registration Date

Jan 08, 2025

Expiry Date

Aug 31, 2029

Product Type

Therapeutic Anesthesia Equipment

Breathing circuit bacterial filter.

Non Electromedic Sterile

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