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SELLA Nasal Oxygen Cannula - Indonesia BPOM Medical Device Registration

SELLA Nasal Oxygen Cannula is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403702522. The device is manufactured by HOSPITAL & HOMECARE IMP. & EXP. CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA AGUNG MANDIRI.

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
SELLA Nasal Oxygen Cannula
Analysis ID: AKL 10403702522

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. DAYA AGUNG MANDIRI

AR Address

JL S. HASANUDIN NO 23 PERUM POLEKO RT 001/001 DESA TAMBUN KEC TAMBUN SELATAN

Registration Date

Jul 09, 2020

Expiry Date

May 13, 2025

Product Type

Therapeutic Anesthesia Equipment

Nasal oxygen cannula.

Non Electromedic Sterile

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