gudid Primary ID: SL 9900 5X digital

LUMENIS (UDI SL 9900 5X digital)

Manufactured by COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The LUMENIS (Model/Catalog Number: SL 9900 5X digital) is a medical device manufactured by COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL. This product is indexed under FDA Product Code / Category Classification HJO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: SL 9900 5X digital
Product Code / EMDN: HJO
Device Name
Database Sync Date: 2026-08-09 09:04:30

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of LUMENIS?

The registered manufacturer of record for LUMENIS is COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL.

What is the Primary UDI-DI identifier for LUMENIS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SL 9900 5X digital.

What classification code is assigned to this device?

This device is registered under product classification code HJO.

Similar Classification Devices (HJO)

Other Devices by COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint