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DELVI CARE Oxygen Mask - Indonesia BPOM Medical Device Registration

DELVI CARE Oxygen Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403321164. The device is manufactured by NINGBO MFLAB MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DELVI PRIMATAMA.

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
DELVI CARE Oxygen Mask
Analysis ID: AKL 10403321164

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. DELVI PRIMATAMA

AR Address

Perum Mutiara Gading Timur Blok A8 No. 7-8 RT 001 RW 031 Kelurahan Mustika Jaya, Kecamatan Mustika Jaya - Kota Bekasi

Registration Date

Mar 23, 2023

Expiry Date

Mar 21, 2026

Product Type

Therapeutic Anesthesia Equipment

Oxygen mask.

Non Electromedic Non Sterile

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