gudid
Primary ID: R8592318
SCT 3000 (UDI R8592318)
Manufactured by Pressalit A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCT 3000 - Primary ID R8592318
Device Regulatory Overview
The SCT 3000 (Model/Catalog Number: R8592318) 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
- R8592318
- Product Code / EMDN
- INQ
- Device Name
- SCT 3000 shower change table, outer measurements 1057 x 1910 mm, lying surface in polyurethane foam, 700 x 1800 mm, graphite gray. Electrically height adjustable with wired remote control, 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 SCT 3000?
The registered manufacturer of record for SCT 3000 is Pressalit A/S.
What is the Primary UDI-DI identifier for SCT 3000?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R8592318.
What classification code is assigned to this device?
This device is registered under product classification code INQ.
Similar Classification Devices (INQ)
Other Devices by Pressalit A/S
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint