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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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Willospon Special — 1 UDI-DI variant, MDD (Will-Pharma BV)

MD Atlas
Will-Pharma BV

Data from EUDAMED, last updated May 31, 2026

Willospon Special

B-08712691209403

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Manufacturer: Will-Pharma BV

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Device characteristics

ImplantableAnimal tissues / cells

Legacy certificates

Certificate number: 1434-MDD-104/2020
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: May 27, 2024

Certificate number: 1434-MDD-105/2020
Type: refdata.legacy.mdd-certificate-type.ii-4
Notified body: POLSKIE CENTRUM BADAN I CERTYFIKACJI S.A. (1434)
Validity: May 27, 2024

Identity & classification

Basic UDI-DI: B-08712691209403
Device name: Willospon Special
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class III
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: Will-Pharma BV
SRN: NL-MF-000006884
Country: Netherlands
Email: info@willpharma.com
Phone: +31(0)204976551

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KSNJMXEC9E9VV0WKZRC0DQJS

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

Willospon® Special08712691209403