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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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GERM B — 2 UDI-DI variants, MDR (XENODERM S.R.L.)

MD Atlas
XENODERM S.R.L.

Data from EUDAMED, last updated May 30, 2026

GERM B

8056098090029DAG1001EL

2 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: XENODERM S.R.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 8056098090029DAG1001EL
Device name: —
Device model: GERM B
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Jun 8, 2023

Manufacturer & authorised representative

Manufacturer

Name: XENODERM S.R.L.
SRN: IT-MF-000031000
Country: Italy
Email: francesco.muollo@xenoderm.it
Phone: +39 0818568081

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H2D40Q18KY6JG9ZMP1H95BM5

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

DGA100108056098090029
DAG035108056098090043