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Geuder GmbH

Germany · Heidelberg

✓ Record-verifiedregistrations found in 9 markets

This company has registrations in United States, Brazil, Saudi Arabia, Canada, Taiwan, Singapore, Australia, Israel, Russia — 9 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

28listed device types

Class I 28Class II 0Class III 0

plus 28 registration records and 1 510(k)

UKUnited KingdomMHRA PARD

pendingnot queried

BRBrazilANVISA

4registered devices

Class I 1Class II 3

this export covers Class I / II only (the cadastro route)

SASaudi ArabiaSFDA

44registered imported devices

low-risk imported devices only; a 2023 snapshot, not updated since

CACanadaMDALL

0active device licences

8 including historic records

TWTaiwanTFDA

2valid device licences

Class I 2

SGSingaporeHSA SMDR

1device registrations

CLASS B 1

KRSouth KoreaMFDS GMP

pendingnot queried

AUAustraliaTGA ARTG

25active ARTG entries

Class I 14IIa 9IIb 2

HKHong KongMDACS

pendingnot queried

ILIsraelAMAR

5registrations

RURussiaRoszdravnadzor

4active registrations

Class 2a 4

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 States28 registration records, 1 510(k), 0 PMA

Brazil4 confirmed, 0 excluded

Saudi Arabia44 confirmed, 0 excluded

Manufacturer names merged into this page: GEUDER AG · Geuder AG

FDA 510(k) clearances by year

12000 · K001125

FDA listed device types

showing 8 of 28

Cannula, Trocar, Ophthalmic 1Ruler, Nearpoint (Punctometer) 1Hook, Ophthalmic 1Marker, Ocular 1Scissors, Ophthalmic 1Clamp, Eyelid, Ophthalmic 1Clamp, Muscle, Ophthalmic 1Snare, Enucleating 1

Registration details (sample)

Market	Identifier	Name	Class / date
US	K001125	GEUDER INJECTOR FOR MORCHER CAPSULAR TENSION RING	2000-10-04
BR	80192019004	F-DECALIN	Class II
BR	80192010065	F-OCTANE	Class II
BR	80192010066	CARTUCHO DMEK	Class II
SA	ME0000003714SFDAA00702	MALONEY KERATOMETER	—
SA	ME0000003714SFDAA00705	FRIEDMANN RONGEUER	—

Geuder GmbH

Registrations by market

How these numbers were verified

Company information

FDA 510(k) clearances by year

FDA listed device types

Registration details (sample)

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