← Back to catalogue

Avea™

FDA UDI

Class II (US FDA UDI)

by Vyaire Medical, Inc.

Identity

Trade Name
AVEA™ FDA UDI
Generic Name
Ventilator breathing circuit, single-use FDA UDI
Device Name
PATIENT BREATHING CIRCUIT 48" FDA UDI
Model / Reference
16044 FDA UDI
Description
PATIENT BREATHING CIRCUIT 48" FDA UDI

Identifiers

Catalog Number
16044 FDA UDI
Primary DI / UDI-DI
10190752199705 FDA UDI
510(k) Number
K103211 FDA UDI
FDA Product Code
CBK FDA UDI
GMDN Term
Ventilator breathing circuit, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5895 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ventilator breathing circuit, single-use

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

Similar devices

Also classified as Ventilator breathing circuit, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI fe940447-1945-4aa9-a959-ec6c8ac9e7a8 36 fields · synced Jun 1, 2026