Medlineunite

FDA UDI

Class II (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: MEDLINEUNITE FDA UDI
Generic Name: Bone nail driver FDA UDI
Device Name: DBD-PIN, TEMP FIX, SMOOTH, 1.1 X 20MM FDA UDI
Model / Reference: MPPF1120 FDA UDI
Description: DBD-PIN, TEMP FIX, SMOOTH, 1.1 X 20MM FDA UDI

Identifiers

Catalog Number: MPPF1120 FDA UDI
Primary DI / UDI-DI: 10888277364462 FDA UDI
FDA Product Code: LHX FDA UDI
LXH FDA UDI
GMDN Term: Bone nail driver FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 870.5800 FDA UDI
888.4540 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Bone nail driver Cannulated surgical drill guiding pin

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

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Also classified as Cannulated surgical drill guiding pin.

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JUGGERLOC 2.9MM GUIDE PIN — Biomet Orthopedics, Inc. · Class II
Hyper-C — Degen Medical · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 7972d0b3-18b2-424d-a984-b28ecd5b2a32 35 fields · synced Jun 8, 2026