HomeGermanyMöller Medical GmbH

Möller Medical GmbH

Germany · Fulda
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Brazil — 2 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
0UDI-DI device records
USUnited StatesFDA openFDA
14listed device types
Class I 8Class II 5Class III 1
plus 15 registration records and 2 510(k)
UKUnited KingdomMHRA PARD
0registered device records
BRBrazilANVISA
16registered devices
Class I 1Class II 15
this export covers Class I / II only (the cadastro route)
SASaudi ArabiaSFDA
0registered 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
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 States15 registration records, 2 510(k), 0 PMA, 2 excluded
Brazil16 confirmed, 0 excluded
Manufacturer names merged into this page: MOELLER MEDICAL GMBH · MÖLLER MEDICAL GMBH · MÖLLER MEDICAL GMBH & CO. KG

Company information

Country
Germany
City
Fulda
Product categories
Manufacturing, Lifecycle & Obsolescence ManagementCDMO (Contract Development and Manufacturing Organization)MedTech (Class I–III)

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

12006 · K053451
12008 · K072793

FDA listed device types

showing 8 of 14
Device, Percutaneous, Biopsy 1Cannula, Surgical, General & Plastic Surgery 1Dispenser, Cement 1Device, Blood Mixing And Blood Weighing 1Needle, Aspiration And Injection, Disposable 1Needle, Aspiration And Injection, Reusable 1Guide, Surgical, Instrument 1Device, Heat-Sealing 1

Registration details (sample)

MarketIdentifierNameClass / date
USK072793LIPOSAT BASIC (INFILTRATION PUMP), MODEL 92-007 6882008-03-04
USK053451LIPOSAT (INFILTRATION PUMP), MODEL 00 002 274; VACUSAT (SUCTION UNIT), MODEL 00 002 252 (220 V), 00 002 318 (110 V);2006-08-25
BR80065320258Sistemas de biópsia da medula ósseaClass II
BR80065320253Instrumento de Biópsia Automático ReutilizávelClass II
BR80065320259Agulhas de localização mamária BLM-1110Class II

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