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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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PODOSTRIPE — 15 UDI-DI variants, MDR (3TO GmbH)

MD Atlas
3TO GmbH

Data from EUDAMED, last updated May 23, 2026

PODOSTRIPE

42516740030000H5

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: 3TO GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42516740030000H5
Device name: PODOSTRIPE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 28, 2026

Manufacturer & authorised representative

Manufacturer

Name: 3TO GmbH
SRN: DE-MF-000017808
Country: Germany
Email: info@3to-gmbh.de
Phone: +49 89 45208330

Variants by status

UDI-DI variants

15 UDI-DI variants

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Applied filters

basicUdiUlid01KQ9WPWJQDYAVEX5JAHY3JNRS

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

312604251674431263
311604251674431164
314104251674431416
311104251674431119
312004251674431201
311704251674431171
314004251674431409
311004251674431102
313704251674431379
312704251674431270
313104251674431317
312104251674431218
313004251674431300
313604251674431362
300004251674430006