gudid
Primary ID: S-1000-SI
Sentinel (UDI S-1000-SI)
Manufactured by ALCOR SCIENTIFIC INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sentinel - Primary ID S-1000-SI
Device Regulatory Overview
The Sentinel (Model/Catalog Number: S-1000-SI) is a medical device manufactured by ALCOR SCIENTIFIC INC.. This product is indexed under FDA Product Code / Category Classification LZH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S-1000-SI
- Product Code / EMDN
- LZH
- Device Name
- Sentinel, Enteral Feeding Pump, 120VAC Type B
- Database Sync Date
- 2026-08-09 09:46:58
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 Sentinel?
The registered manufacturer of record for Sentinel is ALCOR SCIENTIFIC INC..
What is the Primary UDI-DI identifier for Sentinel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S-1000-SI.
What classification code is assigned to this device?
This device is registered under product classification code LZH.
Similar Classification Devices (LZH)
Other Devices by ALCOR SCIENTIFIC INC.
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