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Regard™

FDA UDI

Class I (US FDA UDI)

by Resource Optimization & Innovation, L.l.c.

Identity

Trade Name
Regard™ FDA UDI
Generic Name
Shoe cover FDA UDI
Device Name
COVER BOOT FLD RST REGULAR LARGE FOM NON SKD CTD PP BLUE FDA UDI
Model / Reference
CVRBTTIEL-REG FDA UDI
Description
COVER BOOT FLD RST REGULAR LARGE FOM NON SKD CTD PP BLUE FDA UDI

Identifiers

Catalog Number
CVRBTTIEL-REG FDA UDI
Primary DI / UDI-DI
00326053119132 FDA UDI
FDA Product Code
FXP 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

Yes

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

Regard™ by Resource Optimization & Innovation, L.l.c. — 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 44501c20-2e91-47c2-bd13-0d4a4849be66 34 fields · synced Jun 8, 2026