KIT DIU KOLPLAST

IUD insertion kit · class II · Valid

Registration no.
10237610041
Process no.
25351163009200241
Status
Valid
Device type
IUD insertion kit (KIT PARA INTRODUÇÃO DE DIU)
Risk class
II
Registration holder
KOLPLAST CI LTDA CNPJ 59.231.530/0001-93 · 303 registrations
Manufacturer
KOLPLAST CI LTDA · Brazil
Published
10/06/2002
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 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
Kit DIU Avant Care Pozzi Metal
82441209018
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 16/10/2023 Valid
Kit DIU Avant Care Cheron e Pozzi Metal
82441209019
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 16/10/2023 Valid
Kit Diu Avant Care Plus
82441209004
II VIVA CARE MATERIAL MEDICO HOSPITALAR LTDA 16/11/2022 Valid
Kit DIU
10237610267
I KOLPLAST CI LTDA 29/10/2024 Valid
KIT DIU AUXILIAR
10237610253
I KOLPLAST CI LTDA 05/06/2023 Valid