DeTACH Aortic Cross Clamp Head-Large MI-XCHL-851

GUDID 18022057015881

The DeTACH Detachable Aortic Cross Clamp Head device is a detachable cross clamp head used for temporary or partial occlusion of blood vessels during cardiovascular procedures. The jaws of the device are covered with autraumatic flexible tissue-engagement pads. The upper jaw pivots independently in relation to the pivot jaw actuator arm and the lower/fixed jaw to allow for parralel closure at distances between 5mm and less. The clamp head also incorporates a cam style locking mechanism to lock the jaws in the closed position after dethachment from the delivery device. The DeTACH Detachable Aortic Cross Clamp Head device is available in small, medium and large sizes (55mm, 65mm and 85mm tissue engagement pads respectively) which are packaged and distributed separately. The DeTACH Detachable Aortic Cross Clamp Head device utilizes the DeTACH Delivery Device

CORCYM SRL

Surgical soft-tissue manipulation forceps, scissors-like, single-use
Primary Device ID18022057015881
NIH Device Record Keye5488aef-5f3b-4d1e-9438-a87364a7fb5b
Commercial Distribution StatusIn Commercial Distribution
Brand NameDeTACH Aortic Cross Clamp Head-Large
Version Model NumberMI-XCHL-851
Catalog NumberMI-XCHL-851
Company DUNS441454802
Company NameCORCYM SRL
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS108022057015884 [Primary]
GS118022057015881 [Package]
Contains: 08022057015884
Package: SHELF BOX [6 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXCClamp, Vascular

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2026-02-11
Device Publish Date2026-02-03

Devices Manufactured by CORCYM SRL

18022057015744 - JOSEPH LAMELAS Atrial Lift System2026-02-11 The JOSEPH LAMELAS Atrial Lift System device is a set of 4 disposable surgical instrument components packaged together as a syst
18022057015751 - CUFF Aortic Root Exposure Device2026-02-11 The CUFF device is a flexible surgical retractor designed for exposure and access purposes when inserted into the aortic root an
08022057015761 - JOSEPH LAMELAS Intercostal Retractor System Kit2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
08022057015778 - JOSEPH LAMELAS Intercostal Retractor System Retractor Rack2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
08022057015785 - JOSEPH LAMELAS Intercostal Retractor System Small Blade Set2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
08022057015792 - JOSEPH LAMELAS Intercostal Retractor System Medium Blade Set2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
08022057015808 - JOSEPH LAMELAS Intercostal Retractor System Large Blade Set2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
08022057015815 - JOSEPH LAMELAS Intercostal Retractor System Extra Large Blade Set2026-02-11 The Joseph Lamelas Intercostal Retractor System product is a reusable thoracotomy retractor system. The individual accessory com
© 2026 FDA.report
This site is not affiliated with or endorsed by the FDA.