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STERIMAR Blocked Nose - Indonesia BPOM Medical Device Registration

STERIMAR Blocked Nose is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704813984. 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. KEBAYORAN PHARMA.

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BPOM Registered
Risk Class Kelas Resiko : B
STERIMAR Blocked Nose
Analysis ID: AKL 20704813984

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United Kingdom

Authorized Representative

PT. KEBAYORAN PHARMA

AR Address

Jl. Garuda No.79 Jakarta Pusat, 10610

Registration Date

Jun 10, 2021

Expiry Date

Apr 22, 2026

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Non Sterile

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