gudid
Primary ID: 419
Adtemp (UDI 419)
Manufactured by AMERICAN DIAGNOSTIC CORP
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Adtemp - Primary ID 419
Device Regulatory Overview
The Adtemp (Model/Catalog Number: 419) is a medical device manufactured by AMERICAN DIAGNOSTIC CORP. This product is indexed under FDA Product Code / Category Classification SDV within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 419
- Product Code / EMDN
- SDV
- Device Name
- Adtemp Hypothermia, Digital Thermometer, 10/18 sec, Bulk
- Database Sync Date
- 2026-08-09 09:32:39
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 Adtemp?
The registered manufacturer of record for Adtemp is AMERICAN DIAGNOSTIC CORP.
What is the Primary UDI-DI identifier for Adtemp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 419.
What classification code is assigned to this device?
This device is registered under product classification code SDV.
Similar Classification Devices (SDV)
Other Devices by AMERICAN DIAGNOSTIC CORP
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