HomeGermanyMEDITEC SOURCE GmbH & Co. KG

MEDITEC SOURCE GmbH & Co. KG

Germany · Tuttlingen-Nendingen Baden-Wurttemberg
✓ Record-verifiedregistrations found in 2 markets

This company has registrations in United States, Taiwan — 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
30listed device types
Class I 28Class II 2Class III 0
plus 29 registration records and 0 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
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
1valid device licences
Class I 1
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 States29 registration records, 0 510(k), 0 PMA, 34 excluded
Brazil0 confirmed, 1 excluded
Saudi Arabia0 confirmed, 1 excluded
Canada0 confirmed, 3 excluded
Manufacturer names merged into this page: MEDITEC SOURCE GmbH & Co. KG

Company information

Country
Germany
City
Tuttlingen-Nendingen 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 listed device types

showing 8 of 30
Template 1Rasp 1Forceps 1Elevator 1Scissors, Orthopedic, Surgical 1Handle, Scalpel 1Guide, Surgical, Instrument 1Instrument, Cutting, Orthopedic 1

Similar companies

1st German Health Resilience Conference
Germany · markets 0
3B Scientific GmbH
Germany · markets 1
3R LifeScience GmbH
Germany · markets 0
6th International Sports Pharmacy Symposium
Germany · markets 0
A&D Verpackungsmaschinenbau GmbH
Germany · markets 0
A. u. K. Müller GmbH & Co. KG
Germany · markets 0
Is this your company? Claim the page, add information or report a data error.Claim / report an error →