GUDIDData
eudamed_udi Primary ID: 00884450492482

Merit Medical® (UDI 00884450492482)

Manufactured by Merit Medical Systems, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Merit Medical® - Primary ID 00884450492482

Device Regulatory Overview

The Merit Medical® (Model/Catalog Number: OCSB910P-CE) is a medical device manufactured by Merit Medical Systems, Inc.. This product is indexed under FDA Product Code / Category Classification A020101 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2517-2026 View Full Alert →

Splashwire Hydrophilic Guide Wire: REF: MSWSTDA35150 UDI-DI codes: 00884450529645 00884450529669 00884450529690 REF: MSWSTDA35180 U...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2004-2026 View Full Alert →

Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2003-2026 View Full Alert →

Philips Bridge Prep Kit REF: K12-09098C Sterile EO, Rx ONLY...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
OCSB910P-CE
Product Code / EMDN
A020101
Device Name
Syringes
Database Sync Date
2026-08-09 16:30:42

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Merit Medical®?

The registered manufacturer of record for Merit Medical® is Merit Medical Systems, Inc..

What is the Primary UDI-DI identifier for Merit Medical®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00884450492482.

What classification code is assigned to this device?

This device is registered under product classification code A020101.

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