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AXS Universal Aspiration Tubing - Indonesia BPOM Medical Device Registration

AXS Universal Aspiration Tubing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903520090. The device is manufactured by MEDELA AG from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. NUGRA KARSERA.

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
AXS Universal Aspiration Tubing
Analysis ID: AKL 20903520090

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

MEDELA AG

Country of Origin

Switzerland

Authorized Representative

PT. NUGRA KARSERA

AR Address

Rukan Graha Mas Pemuda, Jalan Pemuda Blok AA/ 10

Registration Date

Jan 22, 2025

Expiry Date

Oct 08, 2029

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus.

Non Electromedic Sterile

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