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VMS Right Anterior Aiming Device (Re-Use)

FDA UDI

Class I (US FDA UDI)

by Elite Surgical Supplies (pty) Ltd

Identity

Trade Name
VMS Right Anterior Aiming Device (Re-Use) FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
VMS Right Anterior Aiming Device (Re-Use): Used to score the femoral neck at 45°. FDA UDI
Model / Reference
VMSAD11 FDA UDI
Description
VMS Right Anterior Aiming Device (Re-Use): Used to score the femoral neck at 45°. FDA UDI

Identifiers

Primary DI / UDI-DI
06009712290383 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

VMS Right Anterior Aiming Device (Re-Use) by Elite Surgical Supplies (pty) Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Elite Surgical Supplies (pty) Ltd

Sources (1)

  • FDA UDI 7a8ecfdc-badc-47b7-8be7-fccbab33275b 33 fields · synced May 30, 2026