gudid
Primary ID: 10-4115
ELEVATOR ARROWHEAD (UDI 10-4115)
Manufactured by W.H. Holden, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ELEVATOR ARROWHEAD - Primary ID 10-4115
Device Regulatory Overview
The ELEVATOR ARROWHEAD (Model/Catalog Number: 10-4115) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification EMJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-4115
- Product Code / EMDN
- EMJ
- Device Name
- Database Sync Date
- 2026-08-09 09:01:13
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 ELEVATOR ARROWHEAD?
The registered manufacturer of record for ELEVATOR ARROWHEAD is W.H. Holden, Inc..
What is the Primary UDI-DI identifier for ELEVATOR ARROWHEAD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-4115.
What classification code is assigned to this device?
This device is registered under product classification code EMJ.
Similar Classification Devices (EMJ)
Other Devices by W.H. Holden, Inc.
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