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emdn_classification Primary ID: W01021312

LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 (UDI W01021312)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 - Primary ID W01021312

Device Regulatory Overview

The LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification W01021312 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-2753-2026 View Full Alert →

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ID: Z-2755-2026 View Full Alert →

FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...

πŸ”’ Compromised Lot & Serial Numbers Locked
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ID: Z-2793-2026 View Full Alert →

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πŸ”’ Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
N/A
Product Code / EMDN
W01021312
Device Name
LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2
Database Sync Date
2026-08-09 16:18:37

Full Regulatory Attributes

πŸ”’ 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 LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2?

The registered manufacturer of record for LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2 is .

What is the Primary UDI-DI identifier for LIPOPROTEIN-ASSOCIATED PHOSPHOLIPASE A2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is W01021312.

What classification code is assigned to this device?

This device is registered under product classification code W01021312.

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