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CORFLO cuBBy

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORFLO cuBBy FDA UDI
Generic Name
Enteral feeding kit, adult/paediatric, sterile FDA UDI
Device Name
Bolus feeding set for use with CORFLO cuBBy FDA UDI
Model / Reference
35-0112 FDA UDI
Description
Bolus feeding set for use with CORFLO cuBBy FDA UDI

Identifiers

Catalog Number
35-0112 FDA UDI
Primary DI / UDI-DI
10815149024438 FDA UDI
FDA Product Code
KNT FDA UDI
GMDN Term
Enteral feeding kit, adult/paediatric, sterile 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

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

Category: Enteral feeding kit, adult/paediatric, sterile

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

Similar devices

Also classified as Enteral feeding kit, adult/paediatric, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Corpak Medsystems

Sources (1)

  • FDA UDI d5ba82e0-86f4-455d-877f-bd7cb2c0171f 35 fields · synced Jun 1, 2026