← Back to catalogue

Vci

FDA UDI

Class II (US FDA UDI)

by Soc Etudes Recherches Fabrication

Identity

Trade Name
VCI FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
NOVAE Dual Mobility Acetabular Cup - VCI screw FDA UDI
Model / Reference
VCI 5 X 25 FDA UDI
Description
NOVAE Dual Mobility Acetabular Cup - VCI screw FDA UDI

Identifiers

Primary DI / UDI-DI
03662200006113 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 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

No

FDA UDI

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic bone screw (non-sliding)

Vci by Soc Etudes Recherches Fabrication — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone screw (non-sliding).

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI e8b31d96-4000-4fbf-a53b-c9c41c6e2c37 33 fields · synced May 31, 2026