eudamed_udi
Primary ID: 10603295107859
GLOBAL ENABLE (UDI 10603295107859)
Manufactured by DePuy Ireland UC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GLOBAL ENABLE - Primary ID 10603295107859
Device Regulatory Overview
The GLOBAL ENABLE (Model/Catalog Number: 2245-10-042) is a medical device manufactured by DePuy Ireland UC. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2245-10-042
- Product Code / EMDN
- L0915
- Device Name
- Hand-Held Surgical Retractor, Reusable
- Database Sync Date
- 2026-08-09 16:30:06
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 GLOBAL ENABLE?
The registered manufacturer of record for GLOBAL ENABLE is DePuy Ireland UC.
What is the Primary UDI-DI identifier for GLOBAL ENABLE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10603295107859.
What classification code is assigned to this device?
This device is registered under product classification code L0915.
Similar Classification Devices (L0915)
Other Devices by DePuy Ireland UC
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