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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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VHO-Osthold-Spange — 6 UDI-DI variants, MDR (Eduard Gerlach GmbH)

MD Atlas
Eduard Gerlach GmbH

Data from EUDAMED, last updated May 23, 2026

VHO-Osthold-Spange

PP09450VHOSPANGE62

6 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: Eduard Gerlach GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: PP09450VHOSPANGE62
Device name: VHO-Osthold-Spange
Device model: VHO-OSTHOLD-Spange Mezzo 0,3 mm
Issuing agency: IFA
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 21, 2026

Manufacturer & authorised representative

Manufacturer

Name: Eduard Gerlach GmbH
SRN: DE-MF-000006590
Country: Germany
Email: info@gehwol.de
Phone: +4957413300

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01KS59NY4NFFKTVWFDWMK4WECJ

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

VHO-Osthold-brace(240)313280002(10)
VHO-Osthold-brace perfect 0,4 maxi313280402
VHO-Osthold-brace Perfect 0,4 Midi313280302
VHO-Osthold-brace Perfect 0,4 mini313280202
VHO-Osthold-brace perfect 0,5 maxi313290402
VHO-Osthold-brace Perfect 0,5 Midi313290302