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Y-Connector for AbbVie PEG 20 FR

FDA UDI

Class II (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name
Y-Connector for AbbVie PEG 20 FR FDA UDI
Generic Name
Jejunostomy tube FDA UDI
Device Name
The saleable unit (device count) is 1, there are 5 Y-Connectors in the saleable unit FDA UDI
Model / Reference
62926 FDA UDI
Description
The saleable unit (device count) is 1, there are 5 Y-Connectors in the saleable unit FDA UDI

Identifiers

Primary DI / UDI-DI
28054083004918 FDA UDI
510(k) Number
K142816 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

Category: Jejunostomy tube

Y-Connector for AbbVie PEG 20 FR by Abbvie Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Jejunostomy tube.

Cleared under the same submission

K142816 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Abbvie Inc.

Sources (1)

  • FDA UDI 3302f8f7-4f71-462e-a6b1-f673046c7cbf 34 fields · synced Jun 8, 2026