GUDIDData
eudamed_udi Primary ID: 00844505012218

LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES (UDI 00844505012218)

Manufactured by Grace Medical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES - Primary ID 00844505012218

Device Regulatory Overview

The LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES (Model/Catalog Number: 6.80.08) is a medical device manufactured by Grace Medical, Inc.. This product is indexed under FDA Product Code / Category Classification L149011 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-2308-2026 View Full Alert →

TITANIUM/FLUOROPLASTIC PISTON 0.6MM DIA X 3.75MM L Model/Catalog Number: 409-375 Product Description: Stapes Prosthesis...

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Technical Specifications

Model Number
6.80.08
Product Code / EMDN
L149011
Device Name
ENT Manual Reusable Surgical Instruments
Database Sync Date
2026-08-09 17:12:06

Full Regulatory Attributes

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{
    "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 LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES?

The registered manufacturer of record for LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES is Grace Medical, Inc..

What is the Primary UDI-DI identifier for LEE NO. 8 DISSECTOR, DOUBLE-ENDED, RIGHT AND LEFT CURVED BLADES?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00844505012218.

What classification code is assigned to this device?

This device is registered under product classification code L149011.

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