GUDIDData
eudamed_udi Primary ID: 00887482101896

Symmetry ® (UDI 00887482101896)

Manufactured by Aspen Surgical Products, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Symmetry ® - Primary ID 00887482101896

Device Regulatory Overview

The Symmetry ® (Model/Catalog Number: 58-1514) is a medical device manufactured by Aspen Surgical Products, Inc.. This product is indexed under FDA Product Code / Category Classification L0205 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-1417-2014 View Full Alert →

7mm Drain Kit, Flat Full Perforated, Saber 100ml Bulb and 3C System Sterile (10/case) Intended for closed wound suction drainage...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-1432-2014 View Full Alert →

15FR Drain Kit Round End Perforated with Trocar and 100ml S-Vac Bulb Evacuator, Sterile (10/case) Intended for closed wound suction drain...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-1424-2014 View Full Alert →

10FR Drain Kit Full Fluted with Trocar and 100ml S-Vac Bulb, Sterile (10/case) Intended for closed wound suction drainage...

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

Technical Specifications

Model Number
58-1514
Product Code / EMDN
L0205
Device Name
Needle Holders
Database Sync Date
2026-08-09 16:28:48

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 Symmetry ®?

The registered manufacturer of record for Symmetry ® is Aspen Surgical Products, Inc..

What is the Primary UDI-DI identifier for Symmetry ®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00887482101896.

What classification code is assigned to this device?

This device is registered under product classification code L0205.

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