Pure Global

EYE-PAK™ Non-Woven Ophthalmic Drape - Indonesia BPOM Medical Device Registration

EYE-PAK™ Non-Woven Ophthalmic Drape is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603026203. The device is manufactured by ALCON RESEARCH, LLC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BINASUKSES CANTEEN.

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 : B
EYE-PAK™ Non-Woven Ophthalmic Drape
Analysis ID: AKL 21603026203

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

BINASUKSES CANTEEN

AR Address

Jl. Pulo Kambing II No. 26 Kawasan Industri Pulogadung, Kel. Jatinegara, Kec. Cakung, Kota Adm. Jakarta Timur, Provinsi DKI Jakarta, Kode Pos 13930

Registration Date

Jun 10, 2024

Expiry Date

Mar 31, 2027

Product Type

Surgical Equipment

Surgical drape and drape accessories.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing