NRCC
NOTICE OF REGISTRATION CONFIRMATION EMAILED
07/03/2023
Voltar para busca
Dado oficial do USPTO
KICKFILE
Sabia que essa marca já está registrada no Estados Unidos?
Antes de investir em nome, identidade e divulgação, valide risco de colisão e estratégia de registro para não perder tempo nem budget.
Active USPTO registrationTipo: VerbalEscritório: US
Diagnóstico de risco e oportunidade
Leitura executiva para decisão de naming, protocolo e monitoramento.
Situação USPTO
Active USPTO registration
Tipo de processo
Pedido e registro
Eventos registrados
24
Atualização mais recente
07/03/2023
Classificação
Registrada
Tipo de marca
Verbal
Classes Nice
42, 45
Data de depósito
13/07/2021
Data de registro
07/03/2023
Data de expiração
-
Ação recomendada
Execute uma análise de colidência completa e valide classes antes de qualquer protocolo ou investimento de marca.
Próximo passo
Esses são os detalhes do processo de registro. Mesmo assim, o monitoramento constante é o que garante tranquilidade de que o seu principal ativo continue protegido.
Dados completos do processo
Campos estruturados da autoridade responsável e do histórico oficial.
Data da situação
07/03/2023
Última transação
07/03/2023
Escritório responsável
United States Patent and Trademark Office
Código da situação
700
Cadastro oficial
Principal Register
Fundamento do pedido
Foreign priority
Código do desenho
4
Tipo de titular
99
Localização do titular
Mölndal, SE
Examinador
BARRETT, LEAH
Unidade examinadora
N80
Localização atual
PUBLICATION AND ISSUE SECTION
Titulares e representantes
Titulares
Kickfile AB
Representantes
John Alumit ALUMIT IP
Classificação técnica
Classes Nice
Classe 42Classe 45
Códigos Vienna
Sem códigos Vienna disponíveis.
Produtos e serviços
Classe 42
Science and technology servicesscientific research in relation to medical devicesin vitro diagnostic productscosmetics and pharmaceuticals; Natural science servicesscientific consulting in relation to medical devicesin vitro diagnostic productscosmetics and pharmaceuticals; Medical and pharmacological research services; Research and development for the pharmaceutical industry; Clinical research and testing services in the field of medical equipment and devices; Advice regarding product development in the field of medical products and devices; Information technology servicestechnological advisory in relation to medical devicesin vitro diagnostic productscosmetics and pharmaceuticals for the pharmaceutical and healthcare industries; Providing temporary use of non-downloadable cloud-based software for managing documents that support compliance for medical devicesin vitro diagnostic productscosmetics and pharmaceuticals; Application service provider (ASP)hosting computer software applications of others; Software as a service (SAAS) services featuring software for cloud-based management of documents supporting compliance for medical devicesin vitro diagnostic productscosmetics and pharmaceuticals; Rental of computer software for cloud-based document management; Electronic data storage; Cloud computing services featuring software for handling and assessing documents; Providing temporary use of non-downloadable cloud-based software for use in the publishing of reportsstudiestemplates and forms involving medical devicesin vitro diagnostic productspharmaceuticals and cosmetics; Providing temporary use of online non-downloadable software for preparing documents for regulatory compliance in the healthcare industry; Providing an onlinecloud-based database of regulatory compliance and validation procedures used in the field of medical equipment and devices
Classe 45
Legal services; Reviewing standards and practices to assure compliance with medical device laws and regulationsin vitro diagnostic product laws and regulationscosmetics laws and regulationspharmaceutical laws and regulations; Regulatory compliance auditing; Information services relating to manufacturing standardsproviding information in the field of regulatory compliance with manufacturing standards; Information services relating to trading standardsproviding information in the field of legal compliance with trading standards; Consultancy services relating to regulatory compliance and validation procedures to ensure compliance with clinical trials in the field of medical equipment and devices; Providing information on state regulatory bodies' examination and approval processes for medical equipment and devices
Publicações
Histórico de despachos e eventos da marca no USPTO.
24 publicações encontradas
R.PR
REGISTERED-PRINCIPAL REGISTER
07/03/2023
NPUB
OFFICIAL GAZETTE PUBLICATION CONFIRMATION E-MAILED
20/12/2022
PUBO
PUBLISHED FOR OPPOSITION
20/12/2022
NONP
NOTIFICATION OF NOTICE OF PUBLICATION E-MAILED
30/11/2022
CNSA
APPROVED FOR PUB - PRINCIPAL REGISTER
16/11/2022
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
08/11/2022
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
07/11/2022
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
07/11/2022
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
07/11/2022
GNRT
NON-FINAL ACTION E-MAILED
07/11/2022
CNRT
NON-FINAL ACTION WRITTEN
07/11/2022
TEME
TEAS/EMAIL CORRESPONDENCE ENTERED
05/10/2022
CRFA
CORRESPONDENCE RECEIVED IN LAW OFFICE
05/10/2022
TROA
TEAS RESPONSE TO OFFICE ACTION RECEIVED
05/10/2022
GNRN
NOTIFICATION OF NON-FINAL ACTION E-MAILED
08/04/2022
GNRT
NON-FINAL ACTION E-MAILED
08/04/2022
CNRT
NON-FINAL ACTION WRITTEN
08/04/2022
DOCK
ASSIGNED TO EXAMINER
31/03/2022
AMPX
PRELIMINARY/VOLUNTARY AMENDMENT - ENTERED
30/12/2021
ALIE
ASSIGNED TO LIE
29/12/2021
PARI
TEAS VOLUNTARY AMENDMENT RECEIVED
23/12/2021
NWOS
NEW APPLICATION OFFICE SUPPLIED DATA ENTERED
17/09/2021
NWAP
NEW APPLICATION ENTERED
16/07/2021
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