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CORFLO Over the Wire Jejunal Tube

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORFLO Over the Wire Jejunal Tube FDA UDI
Generic Name
Jejunostomy tube FDA UDI
Device Name
Jejunal tube with ENFit connectors over the wire for use with CORFLO PEG FDA UDI
Model / Reference
51-1431 FDA UDI
Description
Jejunal tube with ENFit connectors over the wire for use with CORFLO PEG FDA UDI

Identifiers

Catalog Number
51-1431 FDA UDI
Primary DI / UDI-DI
10815149020805 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Jejunostomy 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 10 French FDA UDI
Length — 43 Inch FDA UDI

Category: Jejunostomy tube

CORFLO Over the Wire Jejunal Tube by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Jejunostomy 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 f165b4f0-d0ec-4d96-b5ec-1a25420da052 37 fields · synced Jun 8, 2026