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Gimmi GmbH

US

Last updated May 27, 2026

What Gimmi GmbH makes

Gimmi GmbH manufactures reusable surgical instruments, including monopolar endoscopic electrosurgical electrodes, general-purpose surgical scissors, hand-held retractors, suturing needle holders, laparoscopic access cannulas, trocar blades, soft-tissue manipulation forceps, and orthopaedic rongeurs for joint/limb procedures.

The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Information

Country
US
Address
—
Website
gimmi.de
LinkedIn
—
Facebook
—
Phone
+497461965900
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
316152610

Catalogue (2784)

Page 49 of 56
DeviceModel / ReferenceRegistriesClassStatus
Gimmi AA.1938.16
FDA UDI
Class IActive
Gimmi AA.3222.23
FDA UDI
Class IActive
Gimmi T.8072.06
FDA UDI
Class IIActive
Gimmi AA.1253.14
FDA UDI
Class IActive
Gimmi AA.1309.19
FDA UDI
Class IActive
Gimmi KD.1516.16
FDA UDI
Class IActive
Gimmi GK.2018.02
FDA UDI
Class IActive
Gimmi KH.1832.18
FDA UDI
Class IActive
Gimmi SR.1080.15
EUDAMEDFDA UDI
Class IActive
Gimmi CAM.4140.00
EUDAMEDFDA UDI
Class IIActive
Gimmi AA.1620.10
FDA UDI
Class IActive
Gimmi Z.2935.31
FDA UDI
Class IIActive
Gimmi Z.1635.01
FDA UDI
Class IIActive
Gimmi AD.1213.02
FDA UDI
Class IActive
Gimmi AA.1353.14
FDA UDI
Class IActive
Gimmi B.9129.32
FDA UDI
Class IIActive
Gimmi QO.1160.13
FDA UDI
Class IActive
Gimmi T.8068.12
FDA UDI
Class IIActive
Gimmi QA.1344.07
FDA UDI
Class IActive
Gimmi KH.1910.24
FDA UDI
Class IActive
Gimmi T.8064.11
FDA UDI
Class IIActive
Gimmi AA.1381.19
FDA UDI
Class IActive
Gimmi AB.1463.18
FDA UDI
Class IActive
Gimmi Z.5335.60
FDA UDI
Class IIActive
Gimmi DA.1093.03 AC
FDA UDI
Class IActive
Gimmi DA.1180.15
FDA UDI
Class IActive
Gimmi AD.1735.20
FDA UDI
Class IActive
Gimmi AE.1649.20
FDA UDI
Class IActive
Gimmi GK.2032.02
FDA UDI
Class IActive
Gimmi KH.1880.15
FDA UDI
Class IActive
Gimmi AE.1394.24
FDA UDI
Class IActive
Gimmi CB.1392.30
FDA UDI
Class IActive
Gimmi GK.2034.01
FDA UDI
Class IActive
Gimmi B.9200.02
FDA UDI
Class IIActive
Gimmi AA.1707.10
FDA UDI
Class IActive
Gimmi QO.2050.05
FDA UDI
Class IActive
Gimmi Z.2935.30
FDA UDI
Class IIActive
Gimmi T.8017.27
FDA UDI
Class IIActive
Gimmi AE.1645.24
FDA UDI
Class IActive
Gimmi Z.0005.41
FDA UDI
Class IIActive
Gimmi T.0120.65
FDA UDI
Class IIActive
Gimmi T.0120.59 II
FDA UDI
Class IIActive
Gimmi AE.1470.14
FDA UDI
Class IActive
Gimmi AF.1133.14
FDA UDI
Class IActive
Gimmi AY.1463.10
FDA UDI
Class IActive
Gimmi GK.1929.09
FDA UDI
Class IActive
Gimmi AD.1855.00
FDA UDI
Class IActive
Gimmi AA.1108.14
FDA UDI
Class IActive
Gimmi T.0510.88
FDA UDI
Class IIActive
Gimmi Z.0005.02
FDA UDI
Class IIActive

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Gimmi Gmbh TUTTLINGEN Baden-Wurttemberg · DE FEI 3002807072