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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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Entomed SA201, SA202, SA203, SA204 — 4 UDI-DI variants, MDR

MD Atlas
Auditdata A/S

Data from EUDAMED, last updated May 31, 2026

Entomed SA201, SA202, SA203, SA204

05711781DHF2009ZW

4 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: Auditdata A/S

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Device characteristics

Active deviceMeasuring function

Identity & classification

Basic UDI-DI: 05711781DHF2009ZW
Device name: Entomed SA201, SA202, SA203, SA204
Device model: SA 201, SA202, SA203, SA204
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 28, 2024

Manufacturer & authorised representative

Manufacturer

Name: Auditdata A/S
SRN: DK-MF-000011415
Country: Denmark
Email: compliance@auditdata.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HYZ9XXD2C1PT4BJZA2M9VCD3

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

SA20105711781001227
SA20205711781001234
SA20305711781001241
SA20405711781001258