GUDIDData
eudamed_udi Primary ID: 09421902825798

Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube (UDI 09421902825798)

Manufactured by Adept Medical Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube - Primary ID 09421902825798

Device Regulatory Overview

The Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube (Model/Catalog Number: NZ3257-5) is a medical device manufactured by Adept Medical Ltd. This product is indexed under FDA Product Code / Category Classification Q030399 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-0966-2025 View Full Alert →

Otological Ventilation Tube - T-Tube 9mm - Silicone; Product Code: NZ3309;...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0969-2025 View Full Alert →

Otological Ventilation Tube - Donaldson - Blue Silicone; Product Code: NZ3321;...

🔒 Compromised Lot & Serial Numbers Locked
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ID: Z-0970-2025 View Full Alert →

Otological Ventilation Tube - Donaldson - Double - Blue Silicone; Product Code: NZ3321-2;...

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

Technical Specifications

Model Number
NZ3257-5
Product Code / EMDN
Q030399
Device Name
Myringotomy Kit – no micro ear forceps
Database Sync Date
2026-08-09 17:39:46

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 Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube?

The registered manufacturer of record for Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube is Adept Medical Ltd.

What is the Primary UDI-DI identifier for Myringotomy Kit , with 4mm jaw micro ear forceps and 3 bent suction tube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09421902825798.

What classification code is assigned to this device?

This device is registered under product classification code Q030399.

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