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CORLO Twoomey

FDA UDI

Class II (US FDA UDI)

by Corpak Medsystems

Identity

Trade Name
CORLO Twoomey FDA UDI
Generic Name
Jejunostomy tube FDA UDI
Device Name
Corflo® Twoomey Y-Adaptor 16 FR FDA UDI
Model / Reference
30-6216 FDA UDI
Description
Corflo® Twoomey Y-Adaptor 16 FR FDA UDI

Identifiers

Catalog Number
30-6216 FDA UDI
Primary DI / UDI-DI
10815149024179 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

No

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

Dimensions & Sizes

Size
Catheter Gauge — 16 French FDA UDI

Category: Jejunostomy tube

CORLO Twoomey 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 9c99c51f-4913-4d76-8e91-49f2d66225eb 36 fields · synced May 30, 2026