HomeSpainDESARROLLO E INVESTIGACION MEDICA ARAGONESA, S.L.

DESARROLLO E INVESTIGACION MEDICA ARAGONESA, S.L.

Spain · Calatayud
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 overseas markets. The China NMPA lookup is still pending.

Registrations by market

Each market counts a different unit; figures are not directly comparable
CNChinaNMPA
n/aThis registry lists domestic registrants only
EUEuropean UnionEUDAMED
pendingnot queried
USUnited StatesFDA openFDA
5listed device types
Class I 1Class II 4Class III 0
plus 6 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
3 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
6active device licences
Class II 2Class III 4
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
pendingnot queried
RURussiaRoszdravnadzor
pendingnot queried
Not yet connected: India CDSCO, Indonesia Kemenkes. The public search for Japan PMDA and Vietnam IMDA does not return manufacturer names, so entries cannot be linked to companies coming — where there is no data it is shown as "pending", never estimated.

How these numbers were verified

record-verified

Company-name search in every official database is a substring match and returns same-named but different companies. Each figure below is the count after re-checking every record against the manufacturer name.

United States6 registration records, 0 510(k), 0 PMA
Canada6 confirmed, 0 excluded
Manufacturer names merged into this page: Desarrollo E Investigacion Medica Aragonesa SL · DESARROLLO E INVESTIGACION MEDICA ARAGONESA, S.L. · DESARROLLO E INVESTIGACIÓN MÉDICA ARAGONESA S.L. (DIMA S.L.)

Company information

Country
Spain
City
Calatayud

Fields marked "pending" have not been obtained yet; that does not mean they do not exist. Risk records (litigation, penalties, operating anomalies) are kept internal and not published.

FDA listed device types

Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Female, Mini-Sling 1Mesh, Surgical, For Stress Urinary Incontinence, Male 1Fixation, Non-Absorbable Or Absorbable, For Pelvic Use 1Mesh, Surgical, Synthetic, Urogynecologic, For Stress Urinary Incontinence, Retropubic Or Transobturator 1Instrument, Manual, Surgical, General Use 1

Registration details (sample)

MarketIdentifierNameClass / date
CA85591REMEEX SYSTEM READJUSTMENT KITClass II
CA85753THREAD PASSERClass II
CA85868CONTASURE NEEDLELESSClass III

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