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REMEDI Nasal Oxygen Cannula - Indonesia BPOM Medical Device Registration

REMEDI Nasal Oxygen Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403321041. The device is manufactured by WELL LEAD MEDICAL CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ANUGRAHMITRA SELARAS.

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
REMEDI Nasal Oxygen Cannula
Analysis ID: AKL 10403321041

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ANUGRAHMITRA SELARAS

AR Address

Jl. Agung Niaga IV Blok G.4 No. 54 Kel. Sunter Agung, Kec. Tanjung Priok, Jakarta Utara

Registration Date

Feb 01, 2023

Expiry Date

Jan 29, 2026

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Non Sterile

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