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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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Reconstruction nail — 120 UDI-DI variants, MDR (MEDIN, a.s.)

MD Atlas
MEDIN, a.s.

Data from EUDAMED, last updated May 23, 2026

Reconstruction nail

85917126010101V4

120 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: MEDIN, a.s.

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Device characteristics

Implantable

Legacy certificates

Certificate number: 2023-MDR/QS-028
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Aug 31, 2023 → Aug 31, 2028

Certificate number: 2023-MDR/QS-028/A
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Jan 27, 2025 → Aug 31, 2028

Certificate number: 2023-MDR/TD-028/A
Type: refdata.certificate-mdr-type.technical-documentation
Notified body: 3EC International a.s. (2265)
Validity: Jan 27, 2025 → Aug 31, 2028

Identity & classification

Basic UDI-DI: 85917126010101V4
Device name: Reconstruction nail
Device model: Nail
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 7, 2025

Manufacturer & authorised representative

Manufacturer

Name: MEDIN, a.s.
SRN: CZ-MF-000012371
Country: Czechia
Email: oldrich.pospichal@medin.cz
Phone: +420566684218

Variants by status

UDI-DI variants

120 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01K2247K0MTDZYBGBXZ88KYCRZ

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

No registered UDI-DI variants for this device family.