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PORTEX Suction Catheter - Indonesia BPOM Medical Device Registration

PORTEX Suction Catheter is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903900536. The device is manufactured by SMITHS HEALTHCARE MANUFACTURING SA DE C.V. from Mexico, 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
PORTEX Suction Catheter
Analysis ID: AKL 20903900536

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

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

Aug 30, 2021

Expiry Date

Mar 16, 2025

Product Type

General Hospital Equipment and Other Individuals

Vacuum-powered body fluid suction apparatus.

Non Electromedic Sterile

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