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EAGLE LABS LASIK Cannulae - Indonesia BPOM Medical Device Registration

EAGLE LABS LASIK Cannulae is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203023816. The device is manufactured by EAGLE LABS from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is UNIVERSAL STAR MULTILINK.

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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Risk Class Kelas Resiko : A
EAGLE LABS LASIK Cannulae
Analysis ID: AKL 11203023816

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

EAGLE LABS

Country of Origin

United States

Authorized Representative

UNIVERSAL STAR MULTILINK

AR Address

RUKO SERENADE CENTER BLOK A/27 JL.BOULEVARD GADING SERPONG TANGERANG 15810

Registration Date

Nov 18, 2021

Expiry Date

Jun 02, 2026

Product Type

Surgical Eye Equipment

Manual ophthalmic surgical instrument.

Non Electromedic Sterile

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