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AbbVie Click Adaptor

FDA UDI

Class II (US FDA UDI)

by Abbvie Inc.

Identity

Trade Name
AbbVie Click Adaptor FDA UDI
Generic Name
Jejunostomy tube FDA UDI
Device Name
The saleable unit (device count) is 1, there are 15 click adaptors in the saleable unit FDA UDI
Model / Reference
62922 FDA UDI
Description
The saleable unit (device count) is 1, there are 15 click adaptors in the saleable unit FDA UDI

Identifiers

Primary DI / UDI-DI
08054083004884 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

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

Category: Jejunostomy tube

AbbVie Click Adaptor 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 3b1da207-be16-4d0f-9b9b-079225ddcdb1 34 fields · synced May 30, 2026