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Core

FDA UDI

Class II (US FDA UDI)

by Stryker Corp.

Identity

Trade Name
CORE FDA UDI
Generic Name
Surgical irrigation/aspiration pump, reusable FDA UDI
Device Name
Auto Irrigator Sensor Cable FDA UDI
Model / Reference
5400206001 FDA UDI
Description
Auto Irrigator Sensor Cable FDA UDI

Identifiers

Catalog Number
5400-206-001 FDA UDI
Primary DI / UDI-DI
04546540534163 FDA UDI
FDA Product Code
HBB FDA UDI
GMDN Term
Surgical irrigation/aspiration pump, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4370 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical irrigation/aspiration pump, reusable

Core by Stryker Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical irrigation/aspiration pump, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Stryker Corp.

Sources (1)

  • FDA UDI 09061411-8dff-442d-8344-b4f9eb01b8c6 35 fields · synced May 30, 2026