Pure Global

OPHTEIS ORGANIC 1.8% - Indonesia BPOM Medical Device Registration

OPHTEIS ORGANIC 1.8% is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31203812537. The device is manufactured by RAYNER INTRAOCULAR LENSES LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is BT. Encheval Putera Megatrading.

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
OPHTEIS ORGANIC 1.8%

OPHTEIS BIO 1.8%

Analysis ID: AKL 31203812537

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

United Kingdom

Authorized Representative

BT. Encheval Putera Megatrading

AR Address

JL PULO LENTUT NO. 10 KWS INDUSTRI PULO GADUNG

Registration Date

Nov 26, 2024

Expiry Date

Jun 01, 2029

Product Type

Surgical Eye Equipment

Intraocular fluid.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing