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Cook

FDA UDI

Class II (US FDA UDI)

by Cook Incorporated

Identity

Trade Name
Cook FDA UDI
Generic Name
Peripheral artery cannula FDA UDI
Device Name
Pressure Monitoring Set FDA UDI
Model / Reference
G13489 FDA UDI
Description
Pressure Monitoring Set FDA UDI

Identifiers

Catalog Number
C-KPMS-300 FDA UDI
Primary DI / UDI-DI
00827002134898 FDA UDI
FDA Product Code
DQO FDA UDI
GMDN Term
Peripheral artery cannula 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

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: Peripheral artery cannula

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

Similar devices

Also classified as Peripheral artery cannula.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cook Incorporated

Sources (1)

  • FDA UDI b6a12f44-4104-4fbf-9fc0-c80deefdee8f 36 fields · synced Jun 8, 2026