eudamed_udi Primary ID: 07613327465860

T7 (UDI 07613327465860)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The T7 (Model/Catalog Number: 0416-800-100) is a medical device manufactured by Stryker Instruments. This product is indexed under FDA Product Code / Category Classification T0207 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-1478-2022 View Full Alert →

Stryker 2.3mm Tapered Router, Catalog no. 5820-071-023 instrument used in craniotomy procedures....

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Technical Specifications

Model Number: 0416-800-100
Product Code / EMDN: T0207
Device Name: Personal Protective Equipment: Togas & Hoods
Database Sync Date: 2026-08-09 16:29:34

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 T7?

The registered manufacturer of record for T7 is Stryker Instruments.

What is the Primary UDI-DI identifier for T7?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07613327465860.

What classification code is assigned to this device?

This device is registered under product classification code T0207.

Similar Classification Devices (T0207)

Other Devices by Stryker Instruments

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