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AFENTUBE Aspiration Tubing - Indonesia BPOM Medical Device Registration

AFENTUBE Aspiration Tubing is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903420097. The device is manufactured by WEIHAI HEMO JIRUI BIO-TECHNOLOGY CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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
AFENTUBE Aspiration Tubing
Analysis ID: AKL 20903420097

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. IDS MEDICAL SYSTEMS INDONESIA

AR Address

Gedung Wisma 76, Lantai 17 & 22, Jl. LetJend. S. Parman Kav.76, Kelurahan Slipi, Kecamatan Palmerah, 11410

Registration Date

Jan 27, 2024

Expiry Date

Oct 10, 2026

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus

Non Electromedic Sterile

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