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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Closed-wound drainage kit FDA UDI
Device Name
DRAIN,15FR,3/16,FULL-FLUTED W/ TROCAR FDA UDI
Model / Reference
DYNJWE2264 FDA UDI
Description
DRAIN,15FR,3/16,FULL-FLUTED W/ TROCAR FDA UDI

Identifiers

Catalog Number
DYNJWE2264 FDA UDI
Primary DI / UDI-DI
10080196997633 FDA UDI
FDA Product Code
GBX FDA UDI
GMDN Term
Closed-wound drainage kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4200 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Closed-wound drainage kit

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

Similar devices

Also classified as Closed-wound drainage kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 16f6d457-e680-4963-ba9a-5b6e1d4df11f 36 fields · synced May 30, 2026