FDA UDI In Commercial Distribution 🇺🇸 United States

myEverCup

DI: B8397QJMD6N2Q2171C34A0 · Model: 7KTD9QAT57QJMD6N2Q2171C34A · CASCO BAY MOLDING LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
myEverCup
Primary DI
B8397QJMD6N2Q2171C34A0
Version / Model
7KTD9QAT57QJMD6N2Q2171C34A
Company Name
CASCO BAY MOLDING LTD.
Labeler DUNS
604286695
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-24
Public Version
3
Public Version Date
2020-09-15
Public Version Status
Update
Public Device Record Key
57ebd589-5bfb-41ef-9966-390664754e35

Device Description

Size 1 Mid with Cloth bag

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
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
No

Product Codes

Code Name
HHE Cup, Menstrual

GMDN Terms

Code Name
47728 Menstrual cup, non-latex, reusable

Identifiers

Type ID
Primary B8397QJMD6N2Q2171C34A0