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STERIMAR Allergic Nose - Indonesia BPOM Medical Device Registration

STERIMAR Allergic Nose is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704420032. The device is manufactured by CHURCH & DWIGHT UK LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HYPHENS PHARMA INDONESIA.

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 : B
STERIMAR Allergic Nose
Analysis ID: AKL 20704420032

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. HYPHENS PHARMA INDONESIA

AR Address

Secure Building, Section A Lantai 1, Jalan Raya Protokol Halim Perdana Kusuma, RT.05/RW.10, Kelurahan Halim Perdanakusuma

Registration Date

Jun 11, 2024

Expiry Date

Jan 01, 2029

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Non Sterile

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