gudid
Primary ID: 21520
ReSURGE (UDI 21520)
Manufactured by Sultan Healthcare Inc
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ReSURGE - Primary ID 21520
Device Regulatory Overview
The ReSURGE (Model/Catalog Number: 21520) is a medical device manufactured by Sultan Healthcare Inc. This product is indexed under FDA Product Code / Category Classification FLG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 21520
- Product Code / EMDN
- FLG
- Device Name
- ReSURGE Instrument Cleaning Solution 24x1/2 oz (14.8 mL) Packets
- Database Sync Date
- 2026-08-09 09:03:02
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 ReSURGE?
The registered manufacturer of record for ReSURGE is Sultan Healthcare Inc.
What is the Primary UDI-DI identifier for ReSURGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 21520.
What classification code is assigned to this device?
This device is registered under product classification code FLG.
Similar Classification Devices (FLG)
Other Devices by Sultan Healthcare Inc
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