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Check-Flo Performer

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Check-Flo Performer FDA UDI
Generic Name
Vascular catheter introduction set, nonimplantable FDA UDI
Device Name
Check-Flo Performer Introducer Set FDA UDI
Model / Reference
G57788 FDA UDI
Description
Check-Flo Performer Introducer Set FDA UDI

Identifiers

Catalog Number
RCF-5.0-35-J-01 FDA UDI
Primary DI / UDI-DI
00827002577886 FDA UDI
FDA Product Code
DYB FDA UDI
GMDN Term
Vascular catheter introduction set, nonimplantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1340 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vascular catheter introduction set, nonimplantable

Check-Flo Performer by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Vascular catheter introduction set, nonimplantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 4a42d83d-fec1-440a-946e-35ce7c4b06d1 36 fields · synced Jun 8, 2026