gudid
Primary ID: 93313
Lead Level 3 (UDI 93313)
Manufactured by UTAK LABORATORIES, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lead Level 3 - Primary ID 93313
Device Regulatory Overview
The Lead Level 3 (Model/Catalog Number: 93313) 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
- 93313
- Product Code / EMDN
- DIF
- Device Name
- Lead Level 3
- 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 Lead Level 3?
The registered manufacturer of record for Lead Level 3 is UTAK LABORATORIES, INC..
What is the Primary UDI-DI identifier for Lead Level 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 93313.
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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