GUDIDData
gudid Primary ID: 91.001.1012

GENERIC Surgical Instruments (UDI 91.001.1012)

Manufactured by CTL Medical Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for GENERIC Surgical Instruments - Primary ID 91.001.1012

Device Regulatory Overview

The GENERIC Surgical Instruments (Model/Catalog Number: 91.001.1012) is a medical device manufactured by CTL Medical Corporation. This product is indexed under FDA Product Code / Category Classification HWM 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-2504-2020 View Full Alert →

CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H8mm, Part #018.1908....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2501-2020 View Full Alert →

CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L26, H7mm, Part #018.1307....

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2502-2020 View Full Alert →

CEZANNE II TLIF Bullet-Tip Cage, 8Deg, W11 x L30, H7mm, Part #018.1907....

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

Technical Specifications

Model Number
91.001.1012
Product Code / EMDN
HWM
Device Name
Osteotome Straight, 12
Database Sync Date
2026-08-09 09:16:45

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 GENERIC Surgical Instruments?

The registered manufacturer of record for GENERIC Surgical Instruments is CTL Medical Corporation.

What is the Primary UDI-DI identifier for GENERIC Surgical Instruments?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 91.001.1012.

What classification code is assigned to this device?

This device is registered under product classification code HWM.

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