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Infant Flow™

FDA UDI

Class II (US FDA UDI)

by Vyaire Medical, Inc.

Identity

Trade Name
Infant Flow™ FDA UDI
Generic Name
Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI
Device Name
Infant Flow LP nCPAP Generator without Prongs FDA UDI
Model / Reference
7772000LP FDA UDI
Description
Infant Flow LP nCPAP Generator without Prongs FDA UDI

Identifiers

Catalog Number
7772000LP FDA UDI
Primary DI / UDI-DI
10190752152687 FDA UDI
510(k) Number
K031745 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Inspiratory/expiratory limb respiratory tubing, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5905 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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Inspiratory/expiratory limb respiratory tubing, reusable

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

Similar devices

Also classified as Inspiratory/expiratory limb respiratory tubing, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 73f9aca3-6da0-4cf8-bedb-0c746b22db35 36 fields · synced May 30, 2026