HomeGermanyVOMED VOLZER MEDIZINTECHNIK GMBH & CO.KG

VOMED VOLZER MEDIZINTECHNIK GMBH & CO.KG

Germany · Tuttlingen Baden-Wurttemberg
✓ 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
pendingnot queried
USUnited StatesFDA openFDA
8listed device types
Class I 2Class II 6Class III 0
plus 9 registration records and 3 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
1registered devices
Class II 1
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 States9 registration records, 3 510(k), 0 PMA
Brazil1 confirmed, 0 excluded
Manufacturer names merged into this page: VOMED VOLZER MEDIZINTECHNIK GMBH & CO.KG · VOMED VOLZER MEDIZINTECHNIK GMBH & CO KG

Company information

Country
Germany
City
Tuttlingen 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

32002 · K023019

FDA listed device types

Cystoscope And Accessories, Flexible/Rigid 1Arthroscope 1Hysteroscope (And Accessories) 1Kit, Nephroscope 1Powered Laser Surgical Instrument 1Laparoscope, General & Plastic Surgery 1Instrument, Manual, Surgical, General Use 1Accessories, Arthroscopic 1

Registration details (sample)

MarketIdentifierNameClass / date
USK023019VOMED URETHRA OLIVE, MODELS 1420 000, 1425 000, 1430 0002002-12-10
USK022257VOMED PERIPHERAL VASCULAR ACCESSORIES, MODELS 1010 XXX-7090 XXX & 9006 XXX-9011 XXX2002-10-04
USK022318VOMED ENDOSCOPIC AND UROLOGICAL ACCESSORIES2002-09-19
BR80381210018CANULA DE INSUFLAÇÃO DE VERESSClass II

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