FDA UDI In Commercial Distribution 🇺🇸 United States

DeTACH Aortic Cross Clamp Quick Release Device

DI: 08022057015921 · Model: MI-XCQR-001 · CORCYM SRL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DeTACH Aortic Cross Clamp Quick Release Device
Primary DI
08022057015921
Version / Model
MI-XCQR-001
Catalog Number
MI-XCQR-001
Company Name
CORCYM SRL
Labeler DUNS
441454802
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-02-03
Public Version
1
Public Version Date
2026-02-11
Public Version Status
New
Public Device Record Key
3f02e80e-c5b7-4d1c-8c96-9e8c0b206b07

Device Description

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 utilizes the DeTACH Quick Release.

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
DXC Clamp, Vascular

GMDN Terms

Code Name
62468 Surgical soft-tissue manipulation forceps, scissors-like, reusable

Identifiers

Type ID
Primary 08022057015921

Premarket Submissions

Submission Number Supplement Number
K210006 000