eudamed_udi
Primary ID: 03664492014777
NYLEXOCREP (UDI 03664492014777)
Manufactured by Laboratoires URGO HEALTHCARE
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NYLEXOCREP - Primary ID 03664492014777
Device Regulatory Overview
The NYLEXOCREP (Model/Catalog Number: 3664492014777) is a medical device manufactured by Laboratoires URGO HEALTHCARE. This product is indexed under FDA Product Code / Category Classification M030299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 3664492014777
- Product Code / EMDN
- M030299
- Device Name
- NYLEXOCREP
- Database Sync Date
- 2026-08-09 17:21:14
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 NYLEXOCREP?
The registered manufacturer of record for NYLEXOCREP is Laboratoires URGO HEALTHCARE.
What is the Primary UDI-DI identifier for NYLEXOCREP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03664492014777.
What classification code is assigned to this device?
This device is registered under product classification code M030299.
Similar Classification Devices (M030299)
Other Devices by Laboratoires URGO HEALTHCARE
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