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Cypress

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
Cypress FDA UDI
Generic Name
Shoe cover FDA UDI
Device Name
SHOE COVER, NON-SKID FDA UDI
Model / Reference
35-50 FDA UDI
Description
SHOE COVER, NON-SKID FDA UDI

Identifiers

Primary DI / UDI-DI
10815555020277 FDA UDI
FDA Product Code
OEA FDA UDI
GMDN Term
Shoe cover FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4040 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Shoe cover

Cypress by Mckesson Medical-Surgical Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Shoe cover.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5bcfe742-db36-4d53-a302-1492ca28d980 33 fields · synced May 30, 2026