← Back to catalogue

Dural Elevator

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Dural Elevator FDA UDI
Generic Name
Dura mater dissector FDA UDI
Device Name
Dural Elevator, Flexible Shaft FDA UDI
Model / Reference
07-008-23 FDA UDI
Description
Dural Elevator, Flexible Shaft FDA UDI

Identifiers

Catalog Number
07-008-23 FDA UDI
Primary DI / UDI-DI
04946329052701 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Dura mater dissector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
882.4535 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

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 225 Millimeter FDA UDI

Category: Dura mater dissector

Dural Elevator by Mizuho Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dura mater dissector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI 32d6644b-85aa-48d1-9e44-9cd95dde43c5 36 fields · synced May 30, 2026