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Nonin

FDA UDI

Class II (US FDA UDI)

by Nonin Medical, Inc.

Identity

Trade Name
Nonin FDA UDI
Generic Name
Y-piece breathing circuit connector, single-use FDA UDI
Device Name
Airway Tube Adapter FDA UDI
Model / Reference
9840AAT FDA UDI
Description
Airway Tube Adapter FDA UDI

Identifiers

Primary DI / UDI-DI
00849686071092 FDA UDI
510(k) Number
K982969 FDA UDI
FDA Product Code
CCK FDA UDI
GMDN Term
Y-piece breathing circuit connector, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.1400 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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Y-piece breathing circuit connector, single-use

Nonin by Nonin Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Y-piece breathing circuit connector, single-use.

Cleared under the same submission

K982969 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Nonin Medical, Inc.

Sources (1)

  • FDA UDI d2ee4a70-e5ea-43fc-9230-820408b809ed 35 fields · synced Jun 9, 2026