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VMS Left Anterior Aiming Device - Single Use

FDA UDI

Class I (US FDA UDI)

by Elite Surgical Supplies (pty) Ltd

Identity

Trade Name
VMS Left Anterior Aiming Device - Single Use FDA UDI
Generic Name
Orthopaedic surgical procedure kit, non-medicated, single-use FDA UDI
Device Name
Vertical Measurement System Left Anterior Aiming Device - Single Use: The 45° edge formed by the bend in the device is used as a guide to score the femoral neck prior to the osteotomy of the femoral head. FDA UDI
Model / Reference
VMSAD02 FDA UDI
Description
Vertical Measurement System Left Anterior Aiming Device - Single Use: The 45° edge formed by the bend in the device is used as a guide to score the femoral neck prior to the osteotomy of the femoral head. FDA UDI

Identifiers

Primary DI / UDI-DI
06009708427434 FDA UDI
FDA Product Code
KDC FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, single-use 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

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, single-use

VMS Left Anterior Aiming Device - Single 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, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5e07c128-7ff4-4d04-9a16-87cb216cd223 33 fields · synced May 30, 2026