← Back to catalogue

Ci E

FDA UDI

Class II (US FDA UDI)

by Soc Etudes Recherches Fabrication

Identity

Trade Name
CI E FDA UDI
Generic Name
Non-constrained polyethylene acetabular liner FDA UDI
Device Name
NOVAE Dual Mobility Acetabular Cup - CI E polyethylene liner FDA UDI
Model / Reference
CI 63/28 E FDA UDI
Description
NOVAE Dual Mobility Acetabular Cup - CI E polyethylene liner FDA UDI

Identifiers

Primary DI / UDI-DI
03662200006045 FDA UDI
FDA Product Code
LZO FDA UDI
MEH FDA UDI
GMDN Term
Non-constrained polyethylene acetabular liner 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: Non-constrained polyethylene acetabular liner

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

Similar devices

Also classified as Non-constrained polyethylene acetabular liner.

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 30443f78-6898-4e35-9038-42c93046bd50 33 fields · synced Jun 1, 2026