FDA UDI In Commercial Distribution 🇺🇸 United States

Zenith Flex

DI: 10827002484136 · Model: G48413 · COOK INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zenith Flex
Primary DI
10827002484136
Version / Model
G48413
Catalog Number
TFFB-26-96-ZT
Company Name
COOK INCORPORATED
Labeler DUNS
042823948
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-24
Public Version
6
Public Version Date
2023-01-10
Public Version Status
Update
Public Device Record Key
fe4b032e-e228-4f8b-bd04-66ce1d96ec79

Device Description

Zenith Flex, AAA Endovascular Graft Main Body

Device Characteristics

Single Use
Yes
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
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT

GMDN Terms

Code Name
46777 Abdominal aorta endovascular stent-graft

Identifiers

Type ID
Primary 10827002484136

Customer Contacts

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in dark, dry, cool place.