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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Surgical gown, reusable FDA UDI
Device Name
GOWN,JGR CBN BLK,RED CC,43.5"L,LGE FDA UDI
Model / Reference
MDTZ1001605AE FDA UDI
Description
GOWN,JGR CBN BLK,RED CC,43.5"L,LGE FDA UDI

Identifiers

Catalog Number
MDTZ1001605AE FDA UDI
Primary DI / UDI-DI
20888277418643 FDA UDI
FDA Product Code
OEA FDA UDI
FYA FDA UDI
GMDN Term
Surgical gown, reusable 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical gown, reusable

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

Similar devices

Also classified as Surgical gown, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f4489c2c-b266-498f-899e-0d598cca8010 35 fields · synced May 30, 2026