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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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Pillow — 3 UDI-DI variants, MDR (TRAPUNTIFICIO C.A.T. S.R.L.)

MD Atlas
TRAPUNTIFICIO C.A.T. S.R.L.

Data from EUDAMED, last updated May 31, 2026

Pillow

805559496GNC001F4

3 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: TRAPUNTIFICIO C.A.T. S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805559496GNC001F4
Device name: Pillow
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 23, 2026

Manufacturer & authorised representative

Manufacturer

Name: TRAPUNTIFICIO C.A.T. S.R.L.
SRN: IT-MF-000029712
Country: Italy
Email: info@trapuntificiocat.it
Phone: +39 0461828533

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01KJ5G7M3GBS1NMYHQ1QJ1HB1W

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

GREEN ONDA 275940308055594960317
GREEN SAPONETTA 275939408055594960300
MIND SAPONETTA 280715108055594960324