GUDIDData
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emdn_classification Primary ID: M01020202

SYNTHETIC WOOL WADDING NON-RUBBERISED (UDI M01020202)

Manufactured by

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SYNTHETIC WOOL WADDING NON-RUBBERISED - Primary ID M01020202

Device Regulatory Overview

The SYNTHETIC WOOL WADDING NON-RUBBERISED (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification M01020202 within international Unique Device Identification (UDI) compliance databases.

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Technical Specifications

Model Number
N/A
Product Code / EMDN
M01020202
Device Name
SYNTHETIC WOOL WADDING NON-RUBBERISED
Database Sync Date
2026-08-09 16:18:37

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 SYNTHETIC WOOL WADDING NON-RUBBERISED?

The registered manufacturer of record for SYNTHETIC WOOL WADDING NON-RUBBERISED is .

What is the Primary UDI-DI identifier for SYNTHETIC WOOL WADDING NON-RUBBERISED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is M01020202.

What classification code is assigned to this device?

This device is registered under product classification code M01020202.

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