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Medlineunite

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINEUNITE FDA UDI
Generic Name
Antimicrobial orthopaedic bone pin/wire sleeve FDA UDI
Device Name
TUBE, GUIDEWIRE, 0.9MM X 150MM FDA UDI
Model / Reference
MSGWTUBE1 FDA UDI
Description
TUBE, GUIDEWIRE, 0.9MM X 150MM FDA UDI

Identifiers

Catalog Number
MSGWTUBE1 FDA UDI
Primary DI / UDI-DI
10888277698529 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Antimicrobial orthopaedic bone pin/wire sleeve 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

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Antimicrobial orthopaedic bone pin/wire sleeve

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

Similar devices

Also classified as Antimicrobial orthopaedic bone pin/wire sleeve.

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 fe737f91-7373-4a9d-8ff1-b2de31cd127b 35 fields · synced Jun 8, 2026