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QUIXX Plus - Cold & Flu Blocker - Indonesia BPOM Medical Device Registration

QUIXX Plus - Cold & Flu Blocker is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20704120054. The device is manufactured by NASALEZE LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRANSFARMA MEDICA INDAH.

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BPOM Registered
Risk Class Kelas Resiko : B
QUIXX Plus - Cold & Flu Blocker
Analysis ID: AKL 20704120054

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

NASALEZE LIMITED

Country of Origin

United Kingdom

Authorized Representative

PT. TRANSFARMA MEDICA INDAH

AR Address

Unit 802, 8th Fl., Wisma Pondok Indah 2 JL. Sultan Iskandar Muda Kav V - TA, Pondok Indah.

Registration Date

Jan 05, 2021

Expiry Date

Nov 11, 2025

Product Type

Therapeutic Ear, Nose and Throat Equipment

Nasal irrigation solution

Non Electromedic Non Sterile

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