HomeSpainIberhospitex, S.A.

Iberhospitex, S.A.

Spain · Barcelona
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Brazil, Taiwan, Israel, Russia — 5 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
3510(k) clearances
Class I 0Class II 0Class III 0
plus 0 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
12registered devices
Class I 5Class II 7
15 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
6valid device licences
Class I 2Class II 3Class III 1
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
pendingnot queried
AUAustraliaTGA ARTG
pendingnot queried
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
RURussiaRoszdravnadzor
7active registrations
Class 1 1Class 3 6
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 States0 registration records, 3 510(k), 0 PMA
Brazil12 confirmed, 0 excluded
Manufacturer names merged into this page: IBERHOSPITEX, S.A. · IBERHOSPITEX, S.A

Company information

Country
Spain
City
Barcelona

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 510(k) clearances by year

21988 · K883983
11989 · K883982

Registration details (sample)

MarketIdentifierNameClass / date
USK883982DRENOVAC1989-02-23
USK883983SANIFIX1988-12-13
USK881936OPER-FILM-ADHESIVE MEMBRANE1988-08-31
BR80142340022DRENOFAST - FRASCO PARA ASPIRACAO FECHADA E DRENAGEM DE LIQUIDOSClass II
BR80142349001OPER FIX ESPARADRAPO AUTO ADESIVO HIPOALERGENICOClass I
BR80142340021OPERCAT CURATIVO AUTO-ADESIVO PARA CATETERESClass II

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