HomeGermanyALBER GMBH

ALBER GMBH

Germany · Albstadt Baden-Wurttemberg
✓ Record-verifiedregistrations found in 5 markets

This company has registrations in United States, Saudi Arabia, South Korea, Australia, Israel — 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
4listed device types
Class I 2Class II 2Class III 0
plus 10 registration records and 5 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
4registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
TWTaiwanTFDA
pendingnot queried
SGSingaporeHSA SMDR
pendingnot queried
KRSouth KoreaMFDS GMP
1GMP quality-system certificates
Import 1
AUAustraliaTGA ARTG
2active ARTG entries
Class I 2
HKHong KongMDACS
pendingnot queried
ILIsraelAMAR
1registrations
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 States10 registration records, 5 510(k), 0 PMA, 7 excluded
Brazil0 confirmed, 1 excluded
Saudi Arabia4 confirmed, 1 excluded
Manufacturer names merged into this page: ALBER GMBH · Alber GmbH

Company information

Country
Germany
City
Albstadt Baden-Wurttemberg

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

22016 · K161241
22020 · K192618
12022 · K221215

FDA listed device types

Elevator, Wheelchair, Portable 1Wheelchair, Powered 1Adaptor, Hygiene 1Lift, Patient, Non-Ac-Powered 1

Registration details (sample)

MarketIdentifierNameClass / date
USK221215e-motion M252022-05-24
USK192618e-Motion M252020-11-02
USK192016SMOOV O102020-05-19
SAME0000012323SFDAA00002E-Motion
SAME0000012323SFDAA00004Smoov

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