Versanail®troch Entry Nail Left

FDA UDI

Class II (US FDA UDI)

by Biomet Orthopedics, Inc.

Identity

Trade Name: VERSANAIL®TROCH ENTRY NAIL LEFT FDA UDI
Generic Name: Femur nail, non-sterile FDA UDI
Model / Reference: 1815-10-500 FDA UDI

Identifiers

Catalog Number: 181510500 FDA UDI
Primary DI / UDI-DI: 00887868021183 FDA UDI
FDA Product Code: HWC FDA UDI
JDW FDA UDI
LXT FDA UDI
HTN FDA UDI
KTT FDA UDI
HRS FDA UDI
HTY FDA UDI
HSB FDA UDI
GMDN Term: Femur nail, non-sterile FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3040 FDA UDI
888.3030 FDA UDI
888.3020 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

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: Femur nail, non-sterile

Versanail®troch Entry Nail Left by Biomet Orthopedics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Femur nail, non-sterile.

Flow-Nail™ — Flow-Fx, LLC · Class II
OIC Intramedullary Nail System — ORTHOPAEDIC IMPLANT COMPANY, THE · Class II
GALILEO® TROCHANTERIC NAIL, LEFT, Ø10mm x 30cm x 130° — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class II
AOS ANTEGRADE FEMORAL NAIL, LEFT 13mm x 46cm — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class II
Syntec Femoral Nail System — Syntec Scientific Corp. · Class II
AOS ES™ TROCHANTERIC NAIL, RIGHT 12.5mm x 39cm x 125° — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class II
AOS ANTEGRADE FEMORAL NAIL, RIGHT 9mm x 28cm — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class II
AOS MODULAR NAIL 13.0mm x 46cm — ADVANCED ORTHOPAEDIC SOLUTIONS, INC. · Class II

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: Biomet Orthopedics, Inc.

Sources (1)

FDA UDI 98828917-8ee4-406f-802b-d35b00fcc3ab 35 fields · synced May 30, 2026