gudid
Primary ID: 12-089-19
Cushing Elevator 19cm (UDI 12-089-19)
Manufactured by N S SURGICAL COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cushing Elevator 19cm - Primary ID 12-089-19
Device Regulatory Overview
The Cushing Elevator 19cm (Model/Catalog Number: 12-089-19) 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
- 12-089-19
- Product Code / EMDN
- HTE
- Device Name
- A hand-held, manually-operated surgical instrument used to pry up, lift, and position a bone flap in a neurosurgical procedure upon the skull. Also known as a bone flap elevator it is typically a one-piece instrument that consists of a robust, long, round-nosed, dull blade at the distal working end and a handle at the proximal end. It is typically made of high-grade stainless steel. This is a reusable device.
- Database Sync Date
- 2026-08-09 09:03:58
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 Cushing Elevator 19cm?
The registered manufacturer of record for Cushing Elevator 19cm is N S SURGICAL COMPANY.
What is the Primary UDI-DI identifier for Cushing Elevator 19cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 12-089-19.
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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