← Back to catalogue

Medline

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
Medline FDA UDI
Generic Name
Antimicrobial orthopaedic bone pin/wire sleeve FDA UDI
Device Name
TUBE, GUIDEWIRE, 1.1MM X 150MM FDA UDI
Model / Reference
MSGWTUBE2 FDA UDI
Description
TUBE, GUIDEWIRE, 1.1MM X 150MM FDA UDI

Identifiers

Catalog Number
MSGWTUBE2 FDA UDI
Primary DI / UDI-DI
10888277694774 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
MRI Safety
MR Unsafe FDA UDI

Category: Antimicrobial orthopaedic bone pin/wire sleeve

Medline 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

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

Manufacturer

Manufacturer
Medline Industries, Inc.

Sources (1)

  • FDA UDI 2778dff1-4d4d-499f-9867-01912560af4f 35 fields · synced Jun 8, 2026