GUDIDData
gudid Primary ID: R8595572

CT 4100 (UDI R8595572)

Manufactured by Pressalit A/S

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CT 4100 - Primary ID R8595572

Device Regulatory Overview

The CT 4100 (Model/Catalog Number: R8595572) is a medical device manufactured by Pressalit A/S. This product is indexed under FDA Product Code / Category Classification INQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
R8595572
Product Code / EMDN
INQ
Device Name
CT 4100 change table, lying surface 32'' x 72'', with safety rail, electrically foldable, white. Electrically height adjustable with operating buttons in table front, wall-mounted
Database Sync Date
2026-08-09 09:12:48

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 CT 4100?

The registered manufacturer of record for CT 4100 is Pressalit A/S.

What is the Primary UDI-DI identifier for CT 4100?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R8595572.

What classification code is assigned to this device?

This device is registered under product classification code INQ.

Programmatic Export

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

JSON API Endpoint