Pricing Sign in

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Partners Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Orteză corectoare de statică a… — 56 UDI-DI variants, MDR

MD Atlas
SUPORTH MED SRL

Data from EUDAMED, last updated May 30, 2026

Orteză corectoare de statică a piciorului - Susținător plantar-Podofix carbon

5944759088SUSTPLANTCARB2P

56 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: SUPORTH MED SRL

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5944759088SUSTPLANTCARB2P
Device name: Orteză corectoare de statică a piciorului - Susținător plantar-Podofix carbon
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: SUPORTH MED SRL
SRN: RO-MF-000034720
Country: Romania
Email: reka.suporth@gmail.com

Variants by status

UDI-DI variants

56 UDI-DI variants

Sign in to export

Exports are reserved for signed-in users. Sign in or create an account to continue.

Email

Password

No account yet?

Export results

Applied filters

basicUdiUlid01KSS4HTQKDW7QQ1FGCHEFFF85

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

PED 100 - 3505944759088597
PED 100 - 3605944759088665
PED 100 - 3705944759088337
PED 100 - 3805944759088573
PED 100 - 3905944759088634
PED 100 - 4005944759088443
PED 100 - 4105944759088351
PED 100 - 4205944759088214
PED 100 - 4305944759088559
PED 100 - 4405944759088528
PED 100 - 4505944759088672
PED 100 - 4605944759088474
PED 100 - 4705944759088399
PED 100 - 4805944759088313
PED 101 - 3505944759088221
PED 101 - 3605944759088245
PED 101 - 3705944759088542
PED 101 - 3805944759088344
PED 101 - 3905944759088320
PED 101 - 4005944759088269
PED 101 - 4105944759088726
PED 101 - 4205944759088627
PED 101 - 4305944759088658
PED 101 - 4405944759088368
PED 101 - 4505944759088689

1 2 3