FDA UDI In Commercial Distribution 🇺🇸 United States

Evie

DI: 07290016876017 · Model: EK001 · FERTILIGENT LTD
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Evie
Primary DI
07290016876017
Version / Model
EK001
Catalog Number
EK001
Company Name
FERTILIGENT LTD
Labeler DUNS
533729471
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-11-09
Public Version
3
Public Version Date
2019-01-23
Public Version Status
Update
Public Device Record Key
58986147-2dcd-41d3-b6cf-d656a02fd2be

Device Description

Slow Release Insemination Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MQF Catheter, Assisted Reproduction

GMDN Terms

Code Name
45846 Assisted reproduction transfer catheter/set

Identifiers

Type ID
Primary 07290016876017
Package 17290016876014

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Keep away from sunlight
Type
Special Storage Condition, Specify
Special Conditions
Keep dry