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Ostial Sprit Cannulae

FDA UDI

Class II (US FDA UDI)

by Spyder Medical

Identity

Trade Name
Ostial Sprit Cannulae FDA UDI
Generic Name
Vascular irrigation cannula, coronary artery, single-use FDA UDI
Device Name
Ostial Perfusion Cannula FDA UDI
Model / Reference
CV.CP01005 FDA UDI
Description
Ostial Perfusion Cannula FDA UDI

Identifiers

Catalog Number
CV.CP01005 FDA UDI
Primary DI / UDI-DI
B270CVCP010050 FDA UDI
FDA Product Code
DWF FDA UDI
GMDN Term
Vascular irrigation cannula, coronary artery, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4210 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

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Vascular irrigation cannula, coronary artery, single-use

Ostial Sprit Cannulae by Spyder Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular irrigation cannula, coronary artery, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Spyder Medical

Sources (1)

  • FDA UDI e4686825-387e-4916-b504-cd3ae92d8d8c 34 fields · synced May 31, 2026