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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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REPTACIÓN, GATEO Y POSICIONAMIENTO — 11 UDI-DI variants, MDR

MD Atlas
ORTOTECSA,S.L.

Data from EUDAMED, last updated May 23, 2026

REPTACIÓN, GATEO Y POSICIONAMIENTO

843660217GPVH

11 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: ORTOTECSA,S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843660217GPVH
Device name: REPTACIÓN, GATEO Y POSICIONAMIENTO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: ORTOTECSA,S.L.
SRN: ES-MF-000004786
Country: Spain
Email: info@ortotecsa.com
Phone: +34918719132

Variants by status

UDI-DI variants

11 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KR16E37A6DYD6M9CPC3Y0AG1

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

F.60-4N08436602172159
T.P.133508436602175785
T.P.133008436602175778
T.P.131308436602175747
F.60-2N08436602172142
F.18/2BN08436602170797
F.18/2FN08436602170810
F.18/2CN08436602170803
T.P.132508436602175761
T.P.132008436602175754
F.18/2AN08436602170780