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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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Noviomagus Revision Mesh Proximal Femur — 1 UDI-DI variant, MDD

MD Atlas
Spierings Orthopaedics B.V.

Data from EUDAMED, last updated May 30, 2026

Noviomagus Revision Mesh Proximal Femur

B-08720254007724

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: Spierings Orthopaedics B.V.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 2117262CE01
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: DEKRA Certification B.V. (0344)
Validity: Dec 31, 2027

Identity & classification

Basic UDI-DI: B-08720254007724
Device name: Noviomagus Revision Mesh Proximal Femur
Device model: Noviomagus Revision Mesh Proximal Femur
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: Jan 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: Spierings Orthopaedics B.V.
SRN: NL-MF-000023199
Country: Netherlands
Email: info@spierings.biz
Phone: 0243501603

Variants by status

UDI-DI variants

1 UDI-DI variant

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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

NRM-0906-PF08720254007724