gudid
Primary ID: 400850
Merocel (UDI 400850)
Manufactured by MEDTRONIC XOMED, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Merocel - Primary ID 400850
Device Regulatory Overview
The Merocel (Model/Catalog Number: 400850) is a medical device manufactured by MEDTRONIC XOMED, INC.. This product is indexed under FDA Product Code / Category Classification OCT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 400850
- Product Code / EMDN
- OCT
- Device Name
- SOLUTION 400850 10PK ANTI-FOG
- Database Sync Date
- 2026-08-09 10:01:48
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 Merocel?
The registered manufacturer of record for Merocel is MEDTRONIC XOMED, INC..
What is the Primary UDI-DI identifier for Merocel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 400850.
What classification code is assigned to this device?
This device is registered under product classification code OCT.
Similar Classification Devices (OCT)
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