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ANZON Non-Rebreath Mask - Indonesia BPOM Medical Device Registration

ANZON Non-Rebreath Mask is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403124540. 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 ETERNAL MATESU.

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
ANZON Non-Rebreath Mask
Analysis ID: AKL 10403124540

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

ETERNAL MATESU

AR Address

Jl. Jembatan Tiga No.11C Kel.Penjaringan Kec.Penjaringan - Jakarta Utara Telp : 021-6615716

Registration Date

Feb 16, 2024

Expiry Date

Feb 14, 2027

Product Type

Therapeutic Anesthesia Equipment

Nonrebreathing mask.

Non Electromedic Sterile

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