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GIBECK Humid-Vent Filter Compact - Indonesia BPOM Medical Device Registration

GIBECK Humid-Vent Filter Compact is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403221004. The device is manufactured by TELEFLEX MEDICAL SDN. BHD. from Malaysia, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MURSMEDIC.

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
GIBECK Humid-Vent Filter Compact
Analysis ID: AKL 20403221004

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Malaysia

Authorized Representative

MURSMEDIC

AR Address

Jl. Bukit Gading Raya, Komplek Gading Bukit Indah Blok SA No. 6, Kelurahan Kelapa Gading Barat

Registration Date

Dec 28, 2022

Expiry Date

Dec 31, 2026

Product Type

Therapeutic Anesthesia Equipment

Breathing circuit bacterial filter.

Non Electromedic Sterile

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