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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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ImmunoCAP Allergen — 42 UDI-DI variants, IVDR (Phadia AB)

MD Atlas
Phadia AB

Data from EUDAMED, last updated May 31, 2026

ImmunoCAP Allergen

7333066BUDI0018LZ

42 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class B

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Manufacturer: Phadia AB

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UDI-DI variants

42 UDI-DI variants

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Applied filters

basicUdiUlid01KMJSE7TM3QYA2E5HRFH1K3K8

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

ImmunoCAP Allergen c1, Penicilloyl G07333066001630
ImmunoCAP Allergen c2, Penicilloyl V07333066001647
ImmunoCAP Allergen f45, Yeast07333066002149
ImmunoCAP Allergen f82, Cheese, mold type07333066002804
ImmunoCAP Allergen fx25, Food07333066004693
ImmunoCAP Allergen fx7, Food07333066004563
ImmunoCAP Allergen k87, Allergen component nAsp o 21 Alpha-amylase, Aspergillus oryzae07333066003559
ImmunoCAP Allergen m1, Penicillium chrysogenum07333066001593
ImmunoCAP Allergen m10, Stemphylium herbarum07333066002552
ImmunoCAP Allergen m11, Rhizopus nigricans07333066002569
ImmunoCAP Allergen m12, Aureobasidium pullulans07333066002576
ImmunoCAP Allergen m13, Phoma betae07333066002583
ImmunoCAP Allergen m14, Epicoccum purpurascens07333066002590
ImmunoCAP Allergen m15, Trichoderma viride07333066002606
ImmunoCAP Allergen m16, Curvularia lunata07333066002613
ImmunoCAP Allergen m2, Cladosporium herbarum07333066001128
ImmunoCAP Allergen m202, Acremonium kiliense (Cephalosporium acremonium)07333066004433
ImmunoCAP Allergen m205, Trichophyton rubrum07333066003979
ImmunoCAP Allergen m207, Aspergillus niger07333066004440
ImmunoCAP Allergen m208, Chaetomium globosum07333066008271
ImmunoCAP Allergen m209, Penicillium glabrum07333066008295
ImmunoCAP Allergen m211, Trichophyton ment. var interdigitale07333066008714
ImmunoCAP Allergen m223, Staphylococcal enterotoxin C07333066009810
ImmunoCAP Allergen m227, Malassezia spp.07333066010168
ImmunoCAP Allergen m228, Aspergillus flavus07333066010502

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Device characteristics

ReagentProfessional testing

Identity & classification

Basic UDI-DI: 7333066BUDI0018LZ
Device name: ImmunoCAP Allergen
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class B
Version date: Mar 25, 2026

Manufacturer & authorised representative

Manufacturer

Name: Phadia AB
SRN: SE-MF-000014170
Country: Sweden
Email: RegulatoryAffairs.Uppsala.IDD@thermofisher.com
Phone: +46 18 165000

Variants by status