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Cortrak 2

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORTRAK 2 FDA UDI
Generic Name
Enteral tube tracking system FDA UDI
Device Name
Interconnect cable for CORTRAK 2 FDA UDI
Model / Reference
20-0966 FDA UDI
Description
Interconnect cable for CORTRAK 2 FDA UDI

Identifiers

Catalog Number
20-0966 FDA UDI
Primary DI / UDI-DI
10815149024636 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Enteral tube tracking system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Enteral tube tracking system

Cortrak 2 by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Enteral tube tracking system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corpak Medsystems

Sources (1)

  • FDA UDI 0b745a2d-62ef-4312-8453-2380b2c585c9 35 fields · synced May 30, 2026