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Dukal

FDA UDI

Class I (US FDA UDI)

by Dukal LLC

Identity

Trade Name
Dukal FDA UDI
Generic Name
Scrub suit, single-use FDA UDI
Device Name
CoverSoft™ Scrub Pants Large FDA UDI
Model / Reference
381L FDA UDI
Description
CoverSoft™ Scrub Pants Large FDA UDI

Identifiers

Catalog Number
381L FDA UDI
Primary DI / UDI-DI
10665973026104 FDA UDI
FDA Product Code
LYU FDA UDI
GMDN Term
Scrub suit, single-use 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: Scrub suit, single-use

Dukal by Dukal LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Scrub suit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dukal LLC

Sources (1)

  • FDA UDI 0128deba-d78d-460b-b808-3d73c2bd8e35 35 fields · synced May 30, 2026