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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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Isypan® stitichezza — 1 UDI-DI variant, MDD (LAMP SAN PROSPERO SPA)

MD Atlas
LAMP SAN PROSPERO SPA

Data from EUDAMED, last updated May 30, 2026

Isypan® stitichezza

B-08053504050028

1 UDI-DI variant

MDD [Directive 93/42/EEC on medical devices]Class IIa

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Manufacturer: LAMP SAN PROSPERO SPA

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: EPT 0477.MDD.20/3708.1
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: Eurofins Product Testing Italy S.r.l. (0477)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-08053504050028
Device name: Isypan® stitichezza
Device model: Power for oral solution
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIa
Version date: Jul 4, 2024

Manufacturer & authorised representative

Manufacturer

Name: LAMP SAN PROSPERO SPA
SRN: IT-MF-000039867
Country: Italy
Email: lamp@lamp.it
Phone: 0039 059812211

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01J1YVMJ99559VFVMVJWHRR1N3

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

41000152908053504050028