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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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TRAMA PIATTA — 30 UDI-DI variants, MDR (NEW MEDICAL SERVICE SRL)

MD Atlas
NEW MEDICAL SERVICE SRL

Data from EUDAMED, last updated May 31, 2026

TRAMA PIATTA

805758735714215UC

30 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: NEW MEDICAL SERVICE SRL

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UDI-DI variants

30 UDI-DI variants

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Applied filters

basicUdiUlid01KA8N7TKBYS6XDF9FS8AHD0MH

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

805758735714208057587357142
805758735715908057587357159
805758735716608057587357166
805758735717308057587357173
805758735718008057587357180
805758735719708057587357197
805758735720308057587357203
805758735721008057587357210
805758735722708057587357227
805758735723408057587357234
805758735724108057587357241
805758735725808057587357258
805758735651008057587356510
805758735726508057587357265
805758735727208057587357272
805758735739508057587357395
805758735740108057587357401
805758735741808057587357418
805758735742508057587357425
805758735743208057587357432
805758735744908057587357449
805758735745608057587357456
805758735746308057587357463
805758735729608057587357296
805758735730208057587357302

1 2

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 805758735714215UC
Device name: TRAMA PIATTA
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Nov 17, 2025

Manufacturer & authorised representative

Manufacturer

Name: NEW MEDICAL SERVICE SRL
SRN: IT-MF-000034543
Country: Italy
Email: info@flebysan.it
Phone: +39425474993

Variants by status