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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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PRESSURE BAG — 3 UDI-DI variants, MDR (Intersurgical SpA)

MD Atlas
Intersurgical SpA

Data from EUDAMED, last updated May 31, 2026

PRESSURE BAG

80583230DCPREMISACCAHB

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: Intersurgical SpA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80583230DCPREMISACCAHB
Device name: PRESSURE BAG
Device model: TWINFUSER
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: Intersurgical SpA
SRN: IT-MF-000010729
Country: Italy
Email: s.bellarmi@intersurgical.it
Phone: +390535611073

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KSHWEVBZXJ2H1K15RFBXZ66B

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

T100008058323016958
T50008058323016972
T300008058323016965