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Medline Industries, Inc.

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE INDUSTRIES, INC. FDA UDI
Generic Name
Surgical cap, single-use FDA UDI
Device Name
CAP,BOUFFANT,PROSERIES,HVY WT,BLUE,24" FDA UDI
Model / Reference
NON28533B FDA UDI
Description
CAP,BOUFFANT,PROSERIES,HVY WT,BLUE,24" FDA UDI

Identifiers

Catalog Number
NON28533B FDA UDI
Primary DI / UDI-DI
10080196415939 FDA UDI
FDA Product Code
FYF FDA UDI
GMDN Term
Surgical cap, 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

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: Surgical cap, single-use

Medline Industries, Inc. by Medline Industries, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical cap, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 8884b1bb-122d-40c6-8d79-8fa11193d9a4 35 fields · synced May 30, 2026