THE NEW CE MARKING

Serial Number 88822497
602

Registration Progress

Application Filed
Mar 5, 2020
Under Examination
Approved for Publication
Published for Opposition
Registered

Trademark Image

THE NEW CE MARKING

Basic Information

Serial Number
88822497
Filing Date
March 5, 2020
Abandonment Date
November 30, 2020
Drawing Code
4000

Status Summary

Current Status
Inactive
Status Code
602
Status Date
Dec 14, 2020
Classes
035 042

Rights Holder

MDSS Consulting GmbH

99
Address
Schiffgraben 41
Hannover 30175
DE

Ownership History

MDSS Consulting GmbH

Original Applicant
99
Hannover DE

Legal Representation

Attorney
Terrence L.B. Brown

USPTO Deadlines

No Upcoming Deadlines

No upcoming deadlines found for this trademark.

Application History

10 events
Date Code Type Description Documents
Dec 14, 2020 ABN2 O ABANDONMENT - FAILURE TO RESPOND OR LATE RESPONSE Loading...
Dec 14, 2020 MAB2 E ABANDONMENT NOTICE E-MAILED - FAILURE TO RESPOND Loading...
May 27, 2020 CNRT R NON-FINAL ACTION WRITTEN Loading...
May 27, 2020 GNRT F NON-FINAL ACTION E-MAILED Loading...
May 27, 2020 GNRN O NOTIFICATION OF NON-FINAL ACTION E-MAILED Loading...
May 26, 2020 DOCK D ASSIGNED TO EXAMINER Loading...
Mar 27, 2020 PARI I TEAS VOLUNTARY AMENDMENT RECEIVED Loading...
Mar 27, 2020 TAEA I TEAS AMENDMENT ENTERED BEFORE ATTORNEY ASSIGNED Loading...
Mar 11, 2020 NWOS I NEW APPLICATION OFFICE SUPPLIED DATA ENTERED Loading...
Mar 9, 2020 NWAP I NEW APPLICATION ENTERED Loading...

Detailed Classifications

Class 035
Services of an advisor, examiner, safety officer or a person responsible for compliance with the regulatory regime in the field of medical devices, facilities, instruments, products or procedures, in particular for purposes of compliance with the regulatory regime; outsourcing services, i.e. assistance and representation of manufacturers of medical devices, facilities, instruments or products vis-à-vis third parties and authorities concerning safety issues
First Use Anywhere: 0
First Use in Commerce: 0
Class 042
Consultation in the area of medical devices, facilities, instruments, products or procedures, in particular concerning compliance with regulatory regimes; preparation of expert opinions in the field of medical devices, facilities, instruments, products or procedures, in particular for purposes of compliance with regulatory regimes; implementation of technical assessments that are relevant for approval and safety in the field of medical devices, facilities, instruments or procedures
First Use Anywhere: 0
First Use in Commerce: 0

Classification

International Classes
035 042