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CORFLOTM + CORGRIPTM Combo Pak

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORFLOTM + CORGRIPTM Combo Pak FDA UDI
Generic Name
Nasogastric feeding tube FDA UDI
Device Name
CORFLO feeding tube and NG/NI tube retention system, with ENFit connectors FDA UDI
Model / Reference
45-1362PAK FDA UDI
Description
CORFLO feeding tube and NG/NI tube retention system, with ENFit connectors FDA UDI

Identifiers

Catalog Number
45-1362PAK FDA UDI
Primary DI / UDI-DI
10815149021291 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Nasogastric feeding tube 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

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

Yes

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

No

FDA UDI

Dimensions & Sizes

Size
Length — 36 Inch FDA UDI
Catheter Gauge — 12 French FDA UDI

Category: Nasogastric feeding tube

CORFLOTM + CORGRIPTM Combo Pak by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nasogastric feeding tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corpak Medsystems

Sources (1)

  • FDA UDI 2190b2ae-d559-4b1d-8a92-5cb42a0e8e05 37 fields · synced May 30, 2026