← Back to catalogue

Medline Industries, Inc.

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline Industries, Inc. FDA UDI
Generic Name
General surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
LACERATION TRAY FDA UDI
Model / Reference
DYNDL1754 FDA UDI
Description
LACERATION TRAY FDA UDI

Identifiers

Catalog Number
DYNDL1754 FDA UDI
Primary DI / UDI-DI
10889942159888 FDA UDI
FDA Product Code
MCY FDA UDI
GMDN Term
General surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5075 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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: General surgical procedure kit, non-medicated, reusable

Medline Industries, Inc. presents the LACERATION TRAY, a general surgical procedure kit designed for non-medicated, reusable use in open abdominal surgery and minor dermatological procedures.

Similar devices

Also classified as General surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 5866c938-ff9a-4702-ae37-6111ccb93086 35 fields · synced Oct 6, 2026