CORFLO PEG Kit with snare

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name: CORFLO PEG Kit with snare FDA UDI
Generic Name: Ultraviolet phototherapy unit, professional FDA UDI
Device Name: PEG Safety Kit Push Technique FDA UDI
Model / Reference: 30-4320-S7 FDA UDI
Description: PEG Safety Kit Push Technique FDA UDI

Identifiers

Catalog Number: 30-4320-S7 FDA UDI
Primary DI / UDI-DI: 10815149025350 FDA UDI
FDA Product Code: KNT FDA UDI
GMDN Term: Ultraviolet phototherapy unit, professional 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Ethylene Oxide FDA UDI

Dimensions & Sizes

Size: Catheter Gauge — 20 French FDA UDI

Category: Ultraviolet phototherapy unit, professional

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Corpak Medsystems

Sources (1)

FDA UDI 673cbd3d-a862-492d-be28-080db90cf526 36 fields · synced Jun 8, 2026