eudamed_udi
Primary ID: 04895200307112
Large Cylinder O Ring (UDI 04895200307112)
Manufactured by Regal Prosthesis Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Large Cylinder O Ring - Primary ID 04895200307112
Device Regulatory Overview
The Large Cylinder O Ring (Model/Catalog Number: 2-01-S500-SPN011) is a medical device manufactured by Regal Prosthesis Limited. This product is indexed under FDA Product Code / Category Classification Y062415 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2-01-S500-SPN011
- Product Code / EMDN
- Y062415
- Device Name
- Prosthetic Knee-joints and Hip-joints
- Database Sync Date
- 2026-08-09 16:29:49
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Large Cylinder O Ring?
The registered manufacturer of record for Large Cylinder O Ring is Regal Prosthesis Limited.
What is the Primary UDI-DI identifier for Large Cylinder O Ring?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04895200307112.
What classification code is assigned to this device?
This device is registered under product classification code Y062415.
Similar Classification Devices (Y062415)
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