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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Kruidvat Vaginale Tabletten (10 tablets) — 1 UDI-DI variant, MDD

MD Atlas
S.I.I.T. srl

Data from EUDAMED, last updated May 30, 2026

Kruidvat Vaginale Tabletten (10 tablets)

B-060084507F

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: S.I.I.T. srl

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 426-02-02-DM
Type: refdata.legacy.mdd-certificate-type.v
Notified body: ITALCERT SRL (0426)
Validity: Feb 8, 2024

Identity & classification

Basic UDI-DI: B-060084507F
Device name: Kruidvat Vaginale Tabletten (10 tablets)
Device model: WH24
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: S.I.I.T. srl
SRN: IT-MF-000022188
Country: Italy
Email: surveillance@siit-it.com
Phone: +02 4843521

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KSJBWW5B7YDTRHEKXH5CVW8S

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

Kruidvat Vaginale Tabletten (10 tablets)D-060084507F