HomeGermanyDimeda Instrumente GmbH

Dimeda Instrumente GmbH

Germany · Tuttlingen
✓ Record-verifiedregistrations found in 4 markets

This company has registrations in United States, Taiwan, Australia, Israel — 4 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
253listed device types
Class I 247Class II 6Class III 0
plus 250 registration records and 1 510(k)
UKUnited KingdomMHRA PARD
0registered device records
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
3active ARTG entries
Class I 3
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 States250 registration records, 1 510(k), 0 PMA
Manufacturer names merged into this page: DIMEDA INSTRUMENTE GMBH

Company information

Country
Germany
City
Tuttlingen
Product categories
Clinical Diagnostics & Therapeutic TechnologiesMedical Devices & Clinical EquipmentSurgical systems & instruments

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

12010 · K092827

FDA listed device types

showing 8 of 253
Knife, Margin Finishing, Operative 1Chisel, Surgical, Manual 1Knife, Nasal 1Spreader, Bladder Neck 1Needle, Aspiration And Injection, Disposable 1Stripper, Surgical 1Halter, Head, Traction 1Driver, Surgical, Pin 1

Registration details (sample)

MarketIdentifierNameClass / date
USK092827DIMELA OBSTERICAL FORCEPS, MODEL 72.1 XX XX2010-01-08

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