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Cmatt

FDA UDI

Class I (US FDA UDI)

by Casco Manufacturing Solutions, Inc.

Identity

Trade Name
CMATT FDA UDI
Generic Name
Shoe cover FDA UDI
Device Name
SHOE/ BOOT COVERS (BOOTIE) FDA UDI
Model / Reference
P10002 FDA UDI
Description
SHOE/ BOOT COVERS (BOOTIE) FDA UDI

Identifiers

Catalog Number
P10002 FDA UDI
Primary DI / UDI-DI
00815073028307 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Shoe cover

Cmatt by Casco Manufacturing Solutions, 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 e4036b4c-cb6a-4660-9c84-16b84e7e2a25 35 fields · synced May 30, 2026