Vlp Mini-Mod

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: VLP MINI-MOD FDA UDI
Generic Name: Orthopaedic bone screw (non-sliding) FDA UDI
Device Name: VLP TITANIUM 3.0MM X 48MM OSTEOPENIA SCREW T7 FULLY THREADED FDA UDI
Model / Reference: 74423048 FDA UDI
Description: VLP TITANIUM 3.0MM X 48MM OSTEOPENIA SCREW T7 FULLY THREADED FDA UDI

Identifiers

Catalog Number: 74423048 FDA UDI
Primary DI / UDI-DI: 00885556381748 FDA UDI
FDA Product Code: HRS FDA UDI
GMDN Term: Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3030 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Vlp Mini-Mod by Smith & Nephew, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI 28fda917-3809-4dc6-b46b-f2552c1bf5cd 37 fields · synced Jun 8, 2026