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NES Reprocessed Eagle Eye Platinum Short Tip Stryker

FDA UDI

Class II (US FDA UDI)

by Northeast Scientific, Inc.

Identity

Trade Name
NES Reprocessed Eagle Eye Platinum Short Tip Stryker FDA UDI
Generic Name
Intravascular ultrasound imaging catheter, reprocessed FDA UDI
Device Name
NES Reprocessed Eagle Eye Platinum Short Tip Catheter reprocessed for Stryker (SSS) FDA UDI
Model / Reference
R-S85900PST FDA UDI
Description
NES Reprocessed Eagle Eye Platinum Short Tip Catheter reprocessed for Stryker (SSS) FDA UDI

Identifiers

Catalog Number
R-S85900PST FDA UDI
Primary DI / UDI-DI
B227R85900PST1 FDA UDI
FDA Product Code
OWQ FDA UDI
GMDN Term
Intravascular ultrasound imaging catheter, reprocessed FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1200 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Guidewire Diameter — 0.014 Inch FDA UDI
Introducer Sheath Compatibility — 5 French FDA UDI
Catheter Working Length — 150 Centimeter FDA UDI

Category: Intravascular ultrasound imaging catheter, reprocessed

NES Reprocessed Eagle Eye Platinum Short Tip Stryker by Northeast Scientific, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intravascular ultrasound imaging catheter, reprocessed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 382c9302-5099-45a6-bb58-1a7f0553d35a 37 fields · synced May 29, 2026