gudid Primary ID: SL 9800 3X LED

S4 OPTIK (UDI SL 9800 3X LED)

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 S4 OPTIK (Model/Catalog Number: SL 9800 3X LED) 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 9800 3X LED
Product Code / EMDN: HJO
Device Name: SLIT LAMP SL9800 3X
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 S4 OPTIK?

The registered manufacturer of record for S4 OPTIK is COSTRUZIONI STRUMENTI OFTALMICI C.S.O. SRL.

What is the Primary UDI-DI identifier for S4 OPTIK?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SL 9800 3X LED.

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