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Vaseline

FDA UDI

Class U (US FDA UDI)

by Cardinalhealth

Identity

Trade Name
Vaseline FDA UDI
Generic Name
Dry skin moisture barrier dressing FDA UDI
Device Name
Pure Ultra White Petroleum Jelly,Net Wt. 5 g FDA UDI
Model / Reference
8884433200 FDA UDI
Description
Pure Ultra White Petroleum Jelly,Net Wt. 5 g FDA UDI

Identifiers

Catalog Number
8884433200 FDA UDI
Primary DI / UDI-DI
10884521006867 FDA UDI
FDA Product Code
FRO FDA UDI
GMDN Term
Dry skin moisture barrier dressing FDA UDI

Classification

Device Class
U FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Category: Dry skin moisture barrier dressing

Vaseline by Cardinalhealth — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dry skin moisture barrier dressing.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Cardinalhealth

Sources (1)

  • FDA UDI a9fe54f3-afd0-4806-b0d0-3007a16f9d85 36 fields · synced May 30, 2026