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ROHTO T-BLUE - Indonesia BPOM Medical Device Registration

ROHTO T-BLUE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203420082. The device is manufactured by AUROLAB from India, 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.

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BPOM Registered
Risk Class Kelas Resiko : D
ROHTO T-BLUE
Analysis ID: AKL 31203420082

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

AUROLAB

Country of Origin

India

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

May 21, 2024

Expiry Date

Nov 01, 2028

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

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