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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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COSMETICA PIE PROTESICO, BROWN — 15 UDI-DI variants, MDR

MD Atlas
Ortoiberica S.L.

Data from EUDAMED, last updated May 23, 2026

COSMETICA PIE PROTESICO, BROWN

8431184P19000162

15 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: Ortoiberica S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8431184P19000162
Device name: COSMETICA PIE PROTESICO, BROWN
Device model: P-1900-120
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 19, 2023

Manufacturer & authorised representative

Manufacturer

Name: Ortoiberica S.L.
SRN: ES-MF-000025780
Country: Spain
Email: welcome@ortoiberica.es
Phone: +34985794800

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01HAPFEX522WRG0CTC3TFYNZ1M

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

P-1900-12008431184190010
P-1900-123L08431184191239
P-1900-123R08431184191321
P-1900-124L08431184191246
P-1900-124R08431184191420
P-1900-25L08431184191253
P-1900-126L08431184191260
P-1900-126R08431184191628
P-1900-127L08431184191277
P-1900-127R08431184191727
P-1900-128L08431184191826
P-1900-128R08431184191284
P-1900-129L08431184191291
P-1900-129R08431184191925
P-1900-125R08431184191529