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Spatula

FDA UDI

Class I (US FDA UDI)

by Mizuho Corporation

Identity

Trade Name
Spatula FDA UDI
Generic Name
Neurosurgical retraction system, brain FDA UDI
Device Name
Spatula 4 mm Stainless FDA UDI
Model / Reference
07-959-02 FDA UDI
Description
Spatula 4 mm Stainless FDA UDI

Identifiers

Catalog Number
07-959-02 FDA UDI
Primary DI / UDI-DI
04946329389845 FDA UDI
FDA Product Code
HAO FDA UDI
GMDN Term
Neurosurgical retraction system, brain 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 — 200 Millimeter FDA UDI

Category: Neurosurgical retraction system, brain

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

Similar devices

Also classified as Neurosurgical retraction system, brain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mizuho Corporation

Sources (1)

  • FDA UDI a51d0d2d-4762-4bcb-82ca-a8c5d307618b 36 fields · synced May 30, 2026