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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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Burngel Dressing — 1 UDI-DI variant, MDD (AKLA AB)

MD Atlas
AKLA AB

Data from EUDAMED, last updated May 30, 2026

Burngel Dressing

B-07311410943812DH

1 UDI-DI variant

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

Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Manufacturer: AKLA AB

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 41314724
Type: refdata.legacy.mdd-certificate-type.ii-excluding-4
Notified body: INTERTEK SEMKO AB (0413)
Validity: Dec 31, 2028

Identity & classification

Basic UDI-DI: B-07311410943812DH
Device name: Burngel Dressing
Issuing agency: EUDAMED
Legislation: MDD [Directive 93/42/EEC on medical devices]
Risk class: Class IIb
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: AKLA AB
SRN: SE-MF-000004567
Country: Sweden
Email: info@akla.se
Phone: +4684464730

Variants by status

UDI-DI variants

1 UDI-DI variant

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basicUdiUlid01KSMQDH5VQVRK3TVFMKGA2NSE

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

94381D-07311410943812DH