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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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Comfit AFO — 18 UDI-DI variants, MDR (Embreis AB)

MD Atlas
Embreis AB

Data from EUDAMED, last updated May 31, 2026

Comfit AFO

73401896172QQ

18 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: Embreis AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73401896172QQ
Device name: Comfit AFO
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 20, 2026

Manufacturer & authorised representative

Manufacturer

Name: Embreis AB
SRN: SE-MF-000003023
Country: Sweden
Email: henrietta.hammarlund@embreis.com

Variants by status

UDI-DI variants

18 UDI-DI variants

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Applied filters

basicUdiUlid01KPNFM53PDG65APN7P9ND9QCN

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

E8061PS0507340189639725
E8061PS0307340189639718
E80610007340189642237
E80710007340189642268
E80711707340189603429
E80715707340189603450
E80711307340189603412
E80712707340189603443
E80716707340189603467
E80712307340189603436
E8061-KIT07340189642244
E8062-KIT07340189642251
E80611707340189600060
E80615707340189600091
E80611307340189600077
E80612707340189600046
E80616707340189600084
E80612307340189600053