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Cushing Elevator 19cm

FDA UDI

Class I (US FDA UDI)

by N S Surgical Company

Identity

Trade Name
Cushing Elevator 19cm FDA UDI
Generic Name
Neurosurgical bone flap elevator FDA UDI
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. FDA UDI
Model / Reference
12-089-19 FDA UDI
Description
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. FDA UDI

Identifiers

Catalog Number
12-089-19 FDA UDI
Primary DI / UDI-DI
G25012089190 FDA UDI
FDA Product Code
HTE FDA UDI
GMDN Term
Neurosurgical bone flap elevator FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 19 Centimeter FDA UDI

Category: Neurosurgical bone flap elevator

Cushing Elevator 19cm by N S Surgical Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neurosurgical bone flap elevator.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 66d7c12f-0877-4d31-bf89-7a7979c07f45 35 fields · synced Jun 8, 2026