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Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINE FDA UDI
Generic Name
Suture removal kit FDA UDI
Device Name
SUTURE REMOVAL TRAY 3.5' LITT SCISSORS FDA UDI
Model / Reference
60425 FDA UDI
Description
SUTURE REMOVAL TRAY 3.5' LITT SCISSORS FDA UDI

Identifiers

Catalog Number
60425 FDA UDI
Primary DI / UDI-DI
10193489112054 FDA UDI
FDA Product Code
MCZ FDA UDI
GMDN Term
Suture removal kit 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

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Suture removal kit

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

Similar devices

Also classified as Suture removal kit.

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 1e0399e0-ed0e-4f28-9515-5a5b1f8c53c6 35 fields · synced Jun 8, 2026