gudid
Primary ID: R8591418
SCT 2100 (UDI R8591418)
Manufactured by Pressalit A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SCT 2100 - Primary ID R8591418
Device Regulatory Overview
The SCT 2100 (Model/Catalog Number: R8591418) 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
- R8591418
- Product Code / EMDN
- INQ
- Device Name
- SCT 2100 shower table, outer measurements 900 x 1800 mm, lying surface in coated canvas, 550 x 1650 mm, white. Electrically height adjustable with wired remote control, wall-mounted. Built-in Pressure Sensitive Stop, safety stop, wall-mounted
- Database Sync Date
- 2026-08-09 09:12:48
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SCT 2100?
The registered manufacturer of record for SCT 2100 is Pressalit A/S.
What is the Primary UDI-DI identifier for SCT 2100?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R8591418.
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
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