gudid
Primary ID: 08-036-03
Penfield Elevator (UDI 08-036-03)
Manufactured by N S SURGICAL COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Penfield Elevator - Primary ID 08-036-03
Device Regulatory Overview
The Penfield Elevator (Model/Catalog Number: 08-036-03) is a medical device manufactured by N S SURGICAL COMPANY. This product is indexed under FDA Product Code / Category Classification HTE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 08-036-03
- Product Code / EMDN
- HTE
- Device Name
- A manual surgical instrument designed to lift, position, or pry up (elevate) bone, other anatomical structures, or surgical material/devices during an orthopaedic intervention. It is made of high-grade stainless steel and is available in a wide variety of sizes, designs, and blade shapes. It is typically a robust instrument with a blunted blade with no cutting edge at the distal end that can be pointed, rounded, flat, curved or hook shaped and a handle of various designs at the proximal end. Some types can have special functions, e.g., for angle joint operations or for luxation procedures. This is a reusable device.
- Database Sync Date
- 2026-08-09 09:03:58
Full Regulatory Attributes
🔒 Token Gated
{
"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 Penfield Elevator?
The registered manufacturer of record for Penfield Elevator is N S SURGICAL COMPANY.
What is the Primary UDI-DI identifier for Penfield Elevator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08-036-03.
What classification code is assigned to this device?
This device is registered under product classification code HTE.
Similar Classification Devices (HTE)
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