gudid
Primary ID: BARBS 500 U MAYO V2
BARBITURATES 500 NG/ML (UDI BARBS 500 U MAYO V2)
Manufactured by UTAK LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BARBITURATES 500 NG/ML - Primary ID BARBS 500 U MAYO V2
Device Regulatory Overview
The BARBITURATES 500 NG/ML (Model/Catalog Number: BARBS 500 U MAYO V2) is a medical device manufactured by UTAK LABORATORIES, INC.. This product is indexed under FDA Product Code / Category Classification DIF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BARBS 500 U MAYO V2
- Product Code / EMDN
- DIF
- Device Name
- BARBITURATES 500 NG/ML
- Database Sync Date
- 2026-08-09 09:06:27
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 BARBITURATES 500 NG/ML?
The registered manufacturer of record for BARBITURATES 500 NG/ML is UTAK LABORATORIES, INC..
What is the Primary UDI-DI identifier for BARBITURATES 500 NG/ML?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BARBS 500 U MAYO V2.
What classification code is assigned to this device?
This device is registered under product classification code DIF.
Similar Classification Devices (DIF)
Other Devices by UTAK LABORATORIES, INC.
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