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Cortrak 2eas

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORTRAK 2EAS FDA UDI
Generic Name
Enteral tube tracking system FDA UDI
Device Name
Smart Receiver Unit FDA UDI
Model / Reference
P20-0952 FDA UDI
Description
Smart Receiver Unit FDA UDI

Identifiers

Catalog Number
P20-0952 FDA UDI
Primary DI / UDI-DI
10815149024704 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Enteral tube tracking system

Cortrak 2eas 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 5d32ea1f-91e1-490f-92d6-ba2134593211 35 fields · synced May 30, 2026