FDA UDI In Commercial Distribution 🇺🇸 United States

Aortic Clamp

DI: 10840199535979 · Model: 8560-60 · KOROS U.S.A., INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Aortic Clamp
Primary DI
10840199535979
Version / Model
8560-60
Catalog Number
8560-60
Company Name
KOROS U.S.A., INC.
Labeler DUNS
007928633
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-31
Public Version
1
Public Version Date
2024-02-08
Public Version Status
New
Public Device Record Key
13dcef83-dd8b-4d5c-8c62-2afb3c37784c

Device Description

Aortic Cross Clamp 90 Degree, Accepts 61cm Insert

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
No
PM Exempt
Yes
Has Serial Number
Yes
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
HXD Clamp

GMDN Terms

Code Name
62466 Surgical soft-tissue manipulation forceps, tweezers-like, reusable

Identifiers

Type ID
Direct Marking 00840199535972
Primary 10840199535979

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 9x12mm

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dry place at room temperature