HomeGermanyPTW FREIBURG

PTW FREIBURG

Germany · Freiburg Baden-Wurttemberg
✓ Record-verifiedregistrations found in 3 markets

This company has registrations in United States, Brazil, Canada — 3 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
5listed device types
Class I 3Class II 2Class III 0
plus 14 registration records and 6 510(k)
UKUnited KingdomMHRA PARD
pendingnot queried
BRBrazilANVISA
0registered devices
3 including historic records
SASaudi ArabiaSFDA
0registered imported devices
low-risk imported devices only; a 2023 snapshot, not updated since
CACanadaMDALL
0active device licences
7 including historic records
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 States14 registration records, 6 510(k), 0 PMA
Manufacturer names merged into this page: PTW FREIBURG · PTW-FREIBURG PHYSIKALISCH-TECHNISCHE WERKSTÄTTEN DR. PYCHLAU GMBH · PTW FREIBURG (PHYSIKALISCH TECHNISCHE WERKSTÄTTEN DR. PYCHLAU GMBH)

Company information

Country
Germany
City
Freiburg 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

22017 · K160405
12020 · K191646
12022 · K213370
12024 · K232738
12026 · K252258

FDA listed device types

Accelerator, Linear, Medical 1System, Radiation Therapy, Charged-Particle, Medical 1Instrument, Quality-Assurance, Radiologic 1Phantom, Anthropomorphic, Radiographic 1Source, Calibration, Sealed, Nuclear 1

Registration details (sample)

MarketIdentifierNameClass / date
USK252258VERIQA RT EPID 3D2026-04-15
USK232738BeamDose software (S080053); BEAMSCAN software, option reference dosimetry (S080054.002)2024-05-31
USK213370VERIQA2022-03-30

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