FDA Device Registration & Listing · Lidingo Stockholm, SE · Registration 3015809017
Public RecordDevice ListingExpiry Year: 2026
This page presents structured fields from public FDA datasets.
Registration Header Parameters
Normalized identity and public registration information from FDA records.
Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3015809017
FEI Number
3015809017
Entity Name
MERCADO MEDIC AB
City/State/Country
Lidingo Stockholm,
SE
Establishment Address
Tryffelslingan 14, Lidingo Stockholm 181 57, SE
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Mercado Medic AB (Owner Number: 10091926)
Owner / Operator Contact Address
Tryffelslignan 14, Lidingo, SE-AB 181 57, SE
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A
All Registered Proprietary Names
REAL 9800 EL CoxitREAL 8200 MammographyREAL 9100REAL 9200 Twin/ELREAL 9200 Twin ELREAL 9800REAL 9000REAL Big & Heavy 9200REAL Big & HeavyREAL X-ray 8100REAL 8100 X-rayREAL 8200 Plus MammographyREAL 8200 Plus EL MammographyREAL 9100 PlusREAL Mammography 8200REAL 9200 Big & HeavyREAL X-rayREAL 8100 Plus EL X-rayREAL 8100 Plus X-rayREAL 9800 ELREAL 9400 PlusREA: 9400 Plus ELREAL 9100 Plus ELREAL 9400REAL ChildREAL AdultREAL 9100 AdultREAL Adult 9100REAL 9200REAL 8200
Source Citation & Summary:
This public preview is extracted from openFDA device registration and listing logs under registration number 3015809017.
Last updated year: 2026.
Please use registration number 3015809017 when referencing this establishment in official correspondence.
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