Pure Global

BIOFLEX – Orthoptic Eye Patch For occlusion therapy - Indonesia BPOM Medical Device Registration

BIOFLEX – Orthoptic Eye Patch For occlusion therapy is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902420953. The device is manufactured by SURGITECH INNOVATION PVT,. LTD from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is OPHTHALINDO JAYA MANDIRI.

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 : A
BIOFLEX – Orthoptic Eye Patch For occlusion therapy
Analysis ID: AKL 10902420953

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

India

Authorized Representative

OPHTHALINDO JAYA MANDIRI

AR Address

Superblock Mega Kemayoran (MGK) Blok A No. 8-9 Jl. Angkasa Kav. B-6, Kota Baru, Bandar Kemayoran, Kode Pos 10610, Kel. Gunung Sahari Selatan, Kec. Kemayoran, Kota Jakarta Pusat, Prov. DKI Jakarta

Registration Date

Sep 02, 2024

Expiry Date

Jun 30, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Medical adhesive tape and adhesive bandage, non sterile

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing