GUDIDData
eudamed_udi Primary ID: 00194545063634

Midection, Ring Lk KJT LM/RL 3/16 x 1/2 (UDI 00194545063634)

Manufactured by Becker Orthopedic Appliance Company

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Midection, Ring Lk KJT LM/RL 3/16 x 1/2 - Primary ID 00194545063634

Device Regulatory Overview

The Midection, Ring Lk KJT LM/RL 3/16 x 1/2 (Model/Catalog Number: 1001-C6MS-R) is a medical device manufactured by Becker Orthopedic Appliance Company. This product is indexed under FDA Product Code / Category Classification Y06121201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
1001-C6MS-R
Product Code / EMDN
Y06121201
Device Name
Ring Lock Knee Joint
Database Sync Date
2026-08-09 16:29:26

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 Midection, Ring Lk KJT LM/RL 3/16 x 1/2?

The registered manufacturer of record for Midection, Ring Lk KJT LM/RL 3/16 x 1/2 is Becker Orthopedic Appliance Company.

What is the Primary UDI-DI identifier for Midection, Ring Lk KJT LM/RL 3/16 x 1/2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00194545063634.

What classification code is assigned to this device?

This device is registered under product classification code Y06121201.

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