Medline Unite

FDA UDI

Class I (US FDA UDI)

by Medline Industries, Inc.

Identity

Trade Name: MEDLINE UNITE FDA UDI
Generic Name: Bone nail driver FDA UDI
Device Name: DRIVER, RETAINING, AO/QC, T7 FDA UDI
Model / Reference: MPN30004 FDA UDI
Description: DRIVER, RETAINING, AO/QC, T7 FDA UDI

Identifiers

Catalog Number: MPN30004 FDA UDI
Primary DI / UDI-DI: 10888277690929 FDA UDI
FDA Product Code: HXX FDA UDI
GMDN Term: Bone nail driver 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

FDA UDI

Single Use

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

MRI Safety

MR Unsafe FDA UDI

Category: Bone nail driver

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

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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 I	Pending data

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Manufacturer

Manufacturer: Medline Industries, Inc.

Sources (1)

FDA UDI 74c5f1a7-94b9-4aad-a73f-313a3c87a48f 35 fields · synced May 30, 2026