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Cook

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Cook FDA UDI
Generic Name
Centrally-inserted central venous catheter FDA UDI
Device Name
Femoral Artery Pressure Monitoring Set FDA UDI
Model / Reference
G04448 FDA UDI
Description
Femoral Artery Pressure Monitoring Set FDA UDI

Identifiers

Catalog Number
C-PMS-300-CHILDRENS-A-032988 FDA UDI
Primary DI / UDI-DI
00827002044487 FDA UDI
FDA Product Code
DQY FDA UDI
GMDN Term
Centrally-inserted central venous catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1250 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Category: Centrally-inserted central venous catheter

Cook by Cook Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Centrally-inserted central venous catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI 37d47d4f-92cc-4aa0-9269-181f25e320b2 36 fields · synced Jun 8, 2026