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EZout

FDA UDI

Class I (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
EZout FDA UDI
Generic Name
Surgical saw blade, sagittal, single-use FDA UDI
Device Name
Blade Pack, 42mm FDA UDI
Model / Reference
7812042001K FDA UDI
Description
Blade Pack, 42mm FDA UDI

Identifiers

Catalog Number
7812-042-001K FDA UDI
Primary DI / UDI-DI
07613327294545 FDA UDI
FDA Product Code
HWE FDA UDI
GMDN Term
Surgical saw blade, sagittal, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4820 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Depth — 30.2 Millimeter FDA UDI

Category: Surgical saw blade, sagittal, single-use

EZout by Stryker Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical saw blade, sagittal, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 13c83da0-0f81-4087-b21e-819d3c7f1649 36 fields · synced Jun 1, 2026