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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
Respiratory oxygen therapy system FDA UDI
Device Name
Infant Flow LP Bonnent & Straps, 28-30 cm FDA UDI
Model / Reference
777020 FDA UDI
Description
Infant Flow LP Bonnent & Straps, 28-30 cm FDA UDI

Identifiers

Catalog Number
777020 FDA UDI
Primary DI / UDI-DI
10190752184459 FDA UDI
510(k) Number
K031745 FDA UDI
FDA Product Code
BZD FDA UDI
GMDN Term
Respiratory oxygen therapy system 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: Respiratory oxygen therapy system

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

Similar devices

Also classified as Respiratory oxygen therapy system.

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 77fafcf7-abf5-4c17-a71b-8dfdaf9e5904 37 fields · synced Jun 1, 2026