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ROHTO Fever Patch - Indonesia BPOM Medical Device Registration

ROHTO Fever Patch is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11403412948. The device is manufactured by NEW TAC KASEI CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ROHTO LABORATORIES 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 : A
ROHTO Fever Patch
Analysis ID: AKL 11403412948

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Japan

Authorized Representative

PT. ROHTO LABORATORIES INDONESIA

AR Address

Wisma Barito Pacific Tower B, Lantai 7, Jl. Let. Jend. S. Parman Kav. 62-63

Registration Date

Dec 19, 2021

Expiry Date

Jan 28, 2024

Product Type

Therapeutic Physical Health Equipment

Cold pack.

Non Electromedic Non Sterile

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