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CORFLO PEG Kit

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORFLO PEG Kit FDA UDI
Generic Name
Gastrostomy tube FDA UDI
Device Name
PEG Kit with ENFit Connectors Pull Technique FDA UDI
Model / Reference
50-6020 FDA UDI
Description
PEG Kit with ENFit Connectors Pull Technique FDA UDI

Identifiers

Catalog Number
50-6020 FDA UDI
Primary DI / UDI-DI
10815149021567 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Gastrostomy 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

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
Sterilization Method
Ethylene Oxide FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 20 French FDA UDI

Category: Gastrostomy tube

CORFLO PEG Kit by Corpak Medsystems — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gastrostomy 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 93c56055-3b58-4398-862a-195d8c6daf21 37 fields · synced Jun 8, 2026