International safety notice

Dental X-ray device

Brazil / Anvisa · BRA · Apr 30, 2014

Key facts

Title Dental X-ray device
Regulator Brazil / Anvisa
Country BRA
Brand Sistema de Raios-X Intra-Oral, Modelo CS 2100 e CS 2200 (Antigos KODAK 2100 e KODAK 2200), Registro nº 80378750002. Números de série: WEYA056, WEYA057, WEYA058, WEYA059, WEYA278, WEYA279, WEYA280, WEYA281, WEYA282, WFYA330, WFYA331, WFYA332, XCYA027, XCYA028, XEYA411, XEYA459, XEYA460, XHYC033, XHYC034, XHYC035, XIYC357, XIYC358, XIYC359, XIYC360, XJYC061, XJYC062, XJYC063, XJYC064, XJYC065, XJYC066, XLYC082, XLYC083, XLYC084, XLYC085, YBYC163, YBYC164, YBYC165, YBYC166, YBYC292, YBYC293, YBYC294, YBYC295, YBYC296, YBYC297, YBYC298
Manufacturer DETENTOR DO REGISTRO NO BRASIL CARESTREAM DO BRASIL COMERCIO E SERVIÇOS DE PRODUTOS MEDLCOS LTDA CNPJ 08 546 929 0001 22 ENDEREÇO RUA RUA DR PEDRO LUIZ DE OLIVEIRA COSTA 60 LIMOEIRO 510 JOSÉ DOS CAMPOSSP CEP 12241420
Models YBYC298, YBYC294, XCYA028, WEYA058, WFYA332, WEYA057, XHYC033, XHYC035, YBYC166, XEYA459, XEYA460, XIYC358 and 34 more
Date Apr 30, 2014
Regulator page anvisa.gov.br

At a glance

  • No Recall
  • No Field safety notice
  • 10–99 Matching device models in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

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