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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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PEEP VALVE — 16 UDI-DI variants, MDR (Intersurgical SpA)

MD Atlas
Intersurgical SpA

Data from EUDAMED, last updated May 31, 2026

PEEP VALVE

80583230DCVALVOLEBV

16 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: Intersurgical SpA

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 80583230DCVALVOLEBV
Device name: PEEP VALVE
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 25, 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

16 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS52B946DKBWZ5TSN9MTNV6G

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

SPV2.508058323016118
SPV10308058323016019
SPV10508058323016033
SPV7.508058323016149
SPV15.008058323016101
SPV10.008058323015975
SPV5.008058323016132
SPV12.508058323016071
SPV10008058323015982
SPV10208058323016002
SPV22F08058323050686
SPV10808058323016064
SPV10408058323016026
SPV 2008058323015968
SPV20F08058323016125
SPV30F08058323048256