GUDIDData
eudamed_udi Primary ID: 00840277115829

Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each (UDI 00840277115829)

Manufactured by Innomed, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each - Primary ID 00840277115829

Device Regulatory Overview

The Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each (Model/Catalog Number: T1019) is a medical device manufactured by Innomed, Inc.. This product is indexed under FDA Product Code / Category Classification L0915 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-1753-2024 View Full Alert →

INNOMED CUP REMOVAL STARTER INSTRUMENT, REF 520054, Hip cutter blade cup...

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Technical Specifications

Model Number
T1019
Product Code / EMDN
L0915
Device Name
Retractor
Database Sync Date
2026-08-09 16:29:28

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 Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each?

The registered manufacturer of record for Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each is Innomed, Inc..

What is the Primary UDI-DI identifier for Kolbel Self-Retaining Retractor Blade 36mm x 53mm Each?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840277115829.

What classification code is assigned to this device?

This device is registered under product classification code L0915.

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