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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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Dennis Brown Skinne — 14 UDI-DI variants, MDR (Sahva A/S)

MD Atlas
Sahva A/S

Data from EUDAMED, last updated May 23, 2026

Dennis Brown Skinne

5711433PED001HE

14 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: Sahva A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5711433PED001HE
Device name: Dennis Brown Skinne
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 13, 2026

Manufacturer & authorised representative

Manufacturer

Name: Sahva A/S
SRN: DK-MF-000051700
Country: Denmark
Email: info@sahva.dk
Phone: 70110711

Variants by status

UDI-DI variants

14 UDI-DI variants

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Applied filters

basicUdiUlid01KRGF5EBZ4YG8NFSQKD7Q81WC

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

PO0717305711433055004
PO0717305711433070038
PO0717305711433380342
PO0717305711433155100
PO0717305711433180140
PO0717305711433065027
PO0717305711433165123
PO0717305711433160111
PO0717305711433280246
PO0717305711433060015
PO0717305711433390365
PO0717305711433265229
PO0717305711433270230
PO0717305711433170134