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Medlineunite

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name
MEDLINEUNITE FDA UDI
Generic Name
Cannulated surgical drill guiding pin FDA UDI
Device Name
GUIDEPIN, NON-THREADED, 2.5 X 200MM FDA UDI
Model / Reference
MSG25200 FDA UDI
Description
GUIDEPIN, NON-THREADED, 2.5 X 200MM FDA UDI

Identifiers

Catalog Number
MSG25200 FDA UDI
Primary DI / UDI-DI
10888277139725 FDA UDI
FDA Product Code
LXH FDA UDI
HXX FDA UDI
GMDN Term
Cannulated surgical drill guiding pin FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

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: Cannulated surgical drill guiding pinBone graft harvesting filter

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

Similar devices

Also classified as Bone graft harvesting filter.

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 d956e8b4-a524-4189-86a1-92899be160e2 35 fields · synced May 30, 2026