Pure Global

ROHTO DERMA KIREI + LIDOCAINE - Indonesia BPOM Medical Device Registration

ROHTO DERMA KIREI + LIDOCAINE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602025298. The device is manufactured by HANGZHOU SINGCLEAN MEDICAL PRODUCTS CO., LTD from China, and is classified as Risk Class Kelas Resiko : D. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
ROHTO DERMA KIREI + LIDOCAINE
Analysis ID: AKL 31602025298

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

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

Jan 24, 2023

Expiry Date

Oct 28, 2027

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing