GUDIDData
eudamed_udi Primary ID: 00194545014841

FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit (UDI 00194545014841)

Manufactured by Becker Orthopedic Appliance Company

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit - Primary ID 00194545014841

Device Regulatory Overview

The FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit (Model/Catalog Number: 9006-A6S-R-125-SY) is a medical device manufactured by Becker Orthopedic Appliance Company. This product is indexed under FDA Product Code / Category Classification Y06121203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
9006-A6S-R-125-SY
Product Code / EMDN
Y06121203
Device Name
FullStride
Database Sync Date
2026-08-09 16:48:21

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 FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit?

The registered manufacturer of record for FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit is Becker Orthopedic Appliance Company.

What is the Primary UDI-DI identifier for FullStride, SS, 3/16 x 3/4, Y, GX 125N, RT, Kit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00194545014841.

What classification code is assigned to this device?

This device is registered under product classification code Y06121203.

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