GUDIDData
enforcement Primary ID: Z-0182-2020

Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap (UDI Z-0182-2020)

Manufactured by Andover Healthcare Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap - Primary ID Z-0182-2020

Device Regulatory Overview

The Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap (Model/Catalog Number: Unspecified) is a medical device manufactured by Andover Healthcare Inc.. This product is indexed under FDA Product Code / Category Classification Manufacturer's product or Catalog # 9400S Expiration Date: 01OCT2021-14JUN2022 Lot # CI147V, CI15F1, CI17B9, CI18Y0, CI1FJ3, CI1JCF 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.

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Technical Specifications

Model Number
N/A
Device Name
Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap
Database Sync Date
2026-08-09 10:06:36

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 Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap?

The registered manufacturer of record for Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap is Andover Healthcare Inc..

What is the Primary UDI-DI identifier for Sterile Co-Flex LF2 4" - Product Usage: Single Use secondary wound dressing or compression wrap?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-0182-2020.

What classification code is assigned to this device?

This device is registered under product classification code Manufacturer's product or Catalog # 9400S Expiration Date: 01OCT2021-14JUN2022 Lot # CI147V, CI15F1, CI17B9, CI18Y0, CI1FJ3, CI1JCF.

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