Kit DIU

IUD insertion kit · class I · Valid

Registration no.
10237610267
Process no.
25351423683202404
Status
Valid
Device type
IUD insertion kit (KIT PARA INTRODUÇÃO DE DIU)
Risk class
I
Registration holder
KOLPLAST CI LTDA CNPJ 59.231.530/0001-93 · 303 registrations
Manufacturer
KOLPLAST CI LTDA · Brazil
Published
29/10/2024
Valid until
No expiry (VIGENTE)
Last updated by ANVISA
2026-10-12
Official record
View on ANVISA ↗

Other iud insertion kit registrations (13 in total, see all)

ProductClass HolderPublishedStatus
KIT DIU AUXILIAR
10237610253
I KOLPLAST CI LTDA 05/06/2023 Valid
Kit diu évros
10237610247
I KOLPLAST CI LTDA 30/06/2022 Valid
KIT DIU VAGISPEC
10237610154
I KOLPLAST CI LTDA 18/03/2019 Valid
IUD Instruments (Polypropylene)
80117580723
I EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA 29/10/2018 Valid
IUD Instruments (Polycarbonate)
80117580724
I EMERGO BRAZIL IMPORT IMPORTACAO E DISTRIBUICAO DE PRODUTOS MEDICOS HOSPITALARES LTDA 29/10/2018 Valid
Kit DIU Plus (E)
82441209040
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 04/08/2025 Valid
Kit Diu Avant Care Plus
82441209036
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 07/07/2025 Valid
Kit Diu Auxiliar 1 Avant Care
82441209030
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 08/07/2024 Valid