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VMS Femoral Gauge (Re-Use)

FDA UDI

Class I (US FDA UDI)

by Elite Surgical Supplies (pty) Ltd

Identity

Trade Name
VMS Femoral Gauge (Re-Use) FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
VMS Femoral Gauge (Re-Use): Used to measure the osteotomy height of the femoral neck. FDA UDI
Model / Reference
VMSFG11 FDA UDI
Description
VMS Femoral Gauge (Re-Use): Used to measure the osteotomy height of the femoral neck. FDA UDI

Identifiers

Primary DI / UDI-DI
06009712290437 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

No

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 Femoral Gauge (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

Sources (1)

  • FDA UDI af45d819-f2f0-4fef-a04d-e40f54d0426f 33 fields · synced May 31, 2026