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INTERSURGICAL CLEAR-GUARD Breathing Filter - Indonesia BPOM Medical Device Registration

INTERSURGICAL CLEAR-GUARD Breathing Filter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403718457. The device is manufactured by INTERSURGICAL LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MADESA SEJAHTERA UTAMA.

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
INTERSURGICAL CLEAR-GUARD Breathing Filter
Analysis ID: AKL 20403718457

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

INTERSURGICAL LTD.

Country of Origin

United Kingdom

Authorized Representative

PT. MADESA SEJAHTERA UTAMA

AR Address

JL. GUNUNG SAHARI RAYA 51-A NO.14, GUNUNG SAHARI SELATAN

Registration Date

Mar 13, 2024

Expiry Date

Sep 14, 2026

Product Type

Therapeutic Anesthesia Equipment

Breathing circuit bacterial filter.

Non Electromedic Non Sterile

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