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NEOTECH RAM Cannula - Indonesia BPOM Medical Device Registration

NEOTECH RAM Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403120734. The device is manufactured by NEOTECH PRODUCTS LLC from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANDRA PRIMA JAYA.

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 : A
NEOTECH RAM Cannula
Analysis ID: AKL 10403120734

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

United States

Authorized Representative

PT. ANDRA PRIMA JAYA

AR Address

JL. TANAH ABANG III NO. 19E KEL. PETOJO SELATAN KEC. GAMBIR

Registration Date

Oct 06, 2022

Expiry Date

Dec 31, 2025

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Non Sterile

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