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ERN FINLAN Nasal Aspirator Medical Device - Indonesia BPOM Medical Device Registration

ERN FINLAN Nasal Aspirator Medical Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10704915322. The device is manufactured by HOSPITAL EQUIPMENT MANUFACTURING COMPANY from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is RYNE DUAL SOLE MEDICA.

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
ERN FINLAN Nasal Aspirator Medical Device
Analysis ID: AKL 10704915322

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

India

Authorized Representative

RYNE DUAL SOLE MEDICA

AR Address

JL.TAMAN SARI RAYA NO. 56 SF RT 012 RW 004

Registration Date

May 13, 2024

Expiry Date

Apr 15, 2029

Product Type

Therapeutic Ear, Nose and Throat Equipment

Ear, nose, and throat drug administration device.

Non Electromedic Non Sterile

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