gudid
Primary ID: 13405
Drive (UDI 13405)
Manufactured by Drive Devilbiss Healthcare
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Drive - Primary ID 13405
Device Regulatory Overview
The Drive (Model/Catalog Number: 13405) is a medical device manufactured by Drive Devilbiss Healthcare. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 13405
- Product Code / EMDN
- KZF
- Device Name
- Exam Lamp,GooseNeck,1/cs
- Database Sync Date
- 2026-08-09 09:16:55
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 Drive?
The registered manufacturer of record for Drive is Drive Devilbiss Healthcare.
What is the Primary UDI-DI identifier for Drive?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 13405.
What classification code is assigned to this device?
This device is registered under product classification code KZF.
Similar Classification Devices (KZF)
Other Devices by Drive Devilbiss Healthcare
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