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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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PREMIOFORM — 7 UDI-DI variants, MDR (3TO GmbH)

MD Atlas
3TO GmbH

Data from EUDAMED, last updated May 23, 2026

PREMIOFORM

42516740050000HT

7 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: 42516740050000HT
Device name: PREMIOFORM
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 23, 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

7 UDI-DI variants

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Applied filters

basicUdiUlid01KPWYYRWTT96YP9NTF56RB979

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

512004251674451209
512104251674451216
513104251674451315
513004251674451308
531004251674453104
532004251674453203
500004251674450004