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TELEFLEX Arrow EZ-IO - Indonesia BPOM Medical Device Registration

TELEFLEX Arrow EZ-IO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902127599. The device is manufactured by SPARTONICS WATERTOWN LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. ALFA MEDIKA 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
TELEFLEX Arrow EZ-IO
Analysis ID: AKL 20902127599

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

PT. ALFA MEDIKA INDONESIA

AR Address

RUKO BOULEVARD TEKNO BLOK AA NO. 11, JL. TEKNO WIDYA

Registration Date

Dec 04, 2021

Expiry Date

Dec 31, 2023

Product Type

Therapeutic General and Individual Hospital Equipment

Hypodermic single lumen needle.

Non Radiation Electromedics

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