Pajunk GmbH

Medical device manufacturer in Geisingen, Germ.

19510(k) clearances
0PMA approvals
1recalls

Device types

510(k) clearances

510(k)DeviceDecision
K113207Sono Tap, Tuohy SonoBSP · Traditional 02/29/2012SE
K113209Chiba SonoKNW · Traditional 11/21/2011SE
K060563Epispin, Epispin II Safety, Epispin II, Epispin I, Epispin IVCAZ · Traditional 06/02/2006SE
K053283Uniplex Nanoline Cannula, Plexolong Nanoline Set, Stimulong Nanoline SetCAZ · Special 01/12/2006SE
K053282Adaptable Monopolar Electrodes with Ceramic TipGEI · Special 12/13/2005SE
K043130Modification to Pajunk Stimulong Plus Catheter SetsCAZ · Special 12/21/2004SE
K042979Modification to: Plexalong SetsBSP · Special 12/21/2004SE
K040965Pajunk Tuohy Needles, Quincke Needles, Chiba Needles & Crawford NeedlesBSP · Traditional 09/07/2004SE
K033018Stimulong Plus Catheter Set Model, VariousCAZ · Traditional 05/05/2004SE
K033249Pajunk Modular Handle InstrumentsGCJ · Traditional 03/05/2004SE
K023218Modification to Plexolong SetsBSP · Special 03/24/2003SE
K013041Plexolong SetsCAZ · Traditional 06/11/2002SE
K011308MultistimBXN · Traditional 11/29/2001SE
K012771Trocar Sleeve and Accessories, Models 1287-XX-XXGCJ · Traditional 11/14/2001SE
K011997Modular Valve Handles for Adaptable Tubes, Model 1298-XX-XX, 1295-XX-XXGCJ · Traditional 07/10/2001SE
K000722Unipolar NeedlesBSP · Traditional 03/31/2000SE
K911221Atraumatic Special Sprotte NeedleBSP · Traditional 07/24/1992SE
K911202Atraumatic Standard Sprotte NeedleBSP · Traditional 05/04/1992SE
K911260Atraumatic Standard Sprotte NeedleBSP · Traditional 10/21/1991SE

Recalls

RecallProductInitiated
Z-0234-2020 Class IISPROTTE Lumbar with Introducer, labeled as the following: 1. Sprotte 22G x 90mm w/…Problem with packaging sealing process which affects sterility. 08/30/2019Open, Classified