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OxyKid™

FDA UDI

Class II (US FDA UDI)

by Southmedic Incorporated

Identity

Trade Name
OxyKid™ FDA UDI
Generic Name
Vortex oxygen face mask FDA UDI
Device Name
OxyKid Nebulizer Kit FDA UDI
Model / Reference
OKN-4025-8 FDA UDI
Description
OxyKid Nebulizer Kit FDA UDI

Identifiers

Catalog Number
OKN-4025-8 FDA UDI
Primary DI / UDI-DI
10620974000225 FDA UDI
510(k) Number
K760489 FDA UDI
FDA Product Code
CAF FDA UDI
GMDN Term
Vortex oxygen face mask FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5630 FDA UDI
Commercial Distribution
Not 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

Yes

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

OxyKid™ by Southmedic Incorporated — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K760489 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Southmedic Incorporated

Sources (1)

  • FDA UDI 5ca7af98-2b32-4fb5-87c1-76584f27dfaa 38 fields · synced Jun 8, 2026