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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 instrument interim-placement holder, single-use FDA UDI
Device Name
TRAY,PERFRATD,ALMN,FULL SZ,21.1"X9.5"X2" FDA UDI
Model / Reference
WGN63PA FDA UDI
Description
TRAY,PERFRATD,ALMN,FULL SZ,21.1"X9.5"X2" FDA UDI

Identifiers

Catalog Number
WGN63PA FDA UDI
Primary DI / UDI-DI
10080196915514 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Surgical instrument interim-placement holder, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Instrument tray, reusableSurgical instrument interim-placement holder, 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 instrument interim-placement holder, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 95bb9b5d-ca09-45f4-a76b-05768f47ba59 35 fields · synced Jun 6, 2026