FDA UDI Not in Commercial Distribution 🇺🇸 United States

Zenapro

DI: 10827002237701 · Model: G23770 · COOK BIOTECH INCORPORATED
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zenapro
Primary DI
10827002237701
Version / Model
G23770
Catalog Number
C-HYB-20X30
Company Name
COOK BIOTECH INCORPORATED
Labeler DUNS
945385862
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-03
Public Version
7
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
16c6a18b-ed9b-488e-890b-058ae604b542
Distribution End Date
2018-05-14

Device Description

Zenapro Hybrid Hernia Repair Device

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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
FTL Mesh, surgical, polymeric

GMDN Terms

Code Name
61545 Extra-gynaecological surgical mesh, biologic-polymer composite

Identifiers

Type ID
Primary 10827002237701

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111695 000

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in clean, dry location at room temperature
Type
Storage Environment Temperature
Temperature Range
10 – 30 Degrees Celsius