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Medline

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Surgical/examination garment kit FDA UDI
Device Name
TEST GOWN, XXL, XLONG FDA UDI
Model / Reference
DYNJP2903T FDA UDI
Description
TEST GOWN, XXL, XLONG FDA UDI

Identifiers

Catalog Number
DYNJP2903T FDA UDI
Primary DI / UDI-DI
10888277629301 FDA UDI
FDA Product Code
FYA FDA UDI
GMDN Term
Surgical/examination garment kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical/examination garment kit

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

Similar devices

Also classified as Surgical/examination garment kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 76f7e8bc-8791-4872-b39a-68ec9e528172 35 fields · synced May 30, 2026