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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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Axeltyngd Drake — 5 UDI-DI variants, MDR (Adaptis Spektra AB)

MD Atlas
Adaptis Spektra AB

Data from EUDAMED, last updated May 30, 2026

Axeltyngd Drake

73501429919000PB

5 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: Adaptis Spektra AB

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 73501429919000PB
Device name: Axeltyngd Drake
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 26, 2022

Manufacturer & authorised representative

Manufacturer

Name: Adaptis Spektra AB
SRN: SE-MF-000025764
Country: Sweden
Email: kontakt@butikspektra.se
Phone: +46729743860

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G7VV39Z7B7M0PV1K2WWH085E

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

1900307350142990022
1900207350142990015
1900507350142990893
1900407350142990886
1900107350142990008