gudid
Primary ID: S4000
S40 (UDI S4000)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for S40 - Primary ID S4000
Device Regulatory Overview
The S40 (Model/Catalog Number: S4000) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification MED within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S4000
- Product Code / EMDN
- MED
- Device Name
- The S40 Sterilant Concentrate is a single use peracetic acid-based chemistry used in the SYSTEM 1E and SYSTEM 1 endo Liquid Chemical Sterilant Processing Systems.
- Database Sync Date
- 2026-08-09 09:19:10
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 S40?
The registered manufacturer of record for S40 is STERIS CORPORATION.
What is the Primary UDI-DI identifier for S40?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S4000.
What classification code is assigned to this device?
This device is registered under product classification code MED.
Similar Classification Devices (MED)
Other Devices by STERIS CORPORATION
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