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BIOFLEX © Eye Drape - Indonesia BPOM Medical Device Registration

BIOFLEX © Eye Drape is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603220512. The device is manufactured by SURGITECH INNOVATION PVT. LTD from India, and is classified as Risk Class Kelas Resiko : B. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
BIOFLEX © Eye Drape
Analysis ID: AKL 21603220512

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

OPHTHALINDO JAYA MANDIRI

AR Address

Superblock Mega Kemayoran (MGK) Lantai GF Blok B3 No.1, Jl. Angkasa Kav B-6, Kota Baru, Bandar Kemayoran, Jakarta Pusat 10610

Registration Date

Mar 02, 2022

Expiry Date

Jun 30, 2026

Product Type

Surgical Equipment

Surgical drape and drape accessories.

Non Electromedic Sterile

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