gudid
Primary ID: SA2039
ACE (UDI SA2039)
Manufactured by ALFA WASSERMANN, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACE - Primary ID SA2039
Device Regulatory Overview
The ACE (Model/Catalog Number: SA2039) is a medical device manufactured by ALFA WASSERMANN, INC.. This product is indexed under FDA Product Code / Category Classification KHS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SA2039
- Product Code / EMDN
- KHS
- Device Name
- Carbon Dioxide Reagent
- Database Sync Date
- 2026-08-09 09:49:26
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 ACE?
The registered manufacturer of record for ACE is ALFA WASSERMANN, INC..
What is the Primary UDI-DI identifier for ACE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SA2039.
What classification code is assigned to this device?
This device is registered under product classification code KHS.
Similar Classification Devices (KHS)
Other Devices by ALFA WASSERMANN, INC.
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