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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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Ortesis de miembro superior — 6 UDI-DI variants, MDR (Orliman, S.L.U.)

MD Atlas
Orliman, S.L.U.

Data from EUDAMED, last updated May 31, 2026

Ortesis de miembro superior

84350259ORL20302PK

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: Orliman, S.L.U.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 84350259ORL20302PK
Device name: Ortesis de miembro superior
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 29, 2026

Manufacturer & authorised representative

Manufacturer

Name: Orliman, S.L.U.
SRN: ES-MF-000001598
Country: Spain
Email: eudamed@orliman.es
Phone: +34 962725704

Variants by status

UDI-DI variants

6 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSSN3ENM9JFRWPNZK9VAHMWN

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

MFP-I81#108435025928039
MFP-I81#308435025928053
MFP-D81#108435025927858
MFP-D81#208435025927865
MFP-D81#308435025927872
MFP-I81#208435025928046