FDA UDI In Commercial Distribution 🇺🇸 United States

Flex Cup and Flex Disc

DI: 00851906007255 · Model: Flex Discovery Kit Full Fit · The Flex Company
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
3

Basic Information

Brand Name
Flex Cup and Flex Disc
Primary DI
00851906007255
Version / Model
Flex Discovery Kit Full Fit
Company Name
The Flex Company
Labeler DUNS
080314616
Distribution Status
In Commercial Distribution
Device Count in Pkg
3
Record Status
Published
Publish Date
2019-03-14
Public Version
4
Public Version Date
2022-07-22
Public Version Status
Update
Public Device Record Key
546c79bc-5626-4de1-ae4e-68e97ea5320b

Device Description

Flex Cup Size 2 and 2 Flex Discs (English only)

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
47723 Menstrual cup, non-latex, single-use

Identifiers

Type ID
Primary 00851906007255
Unit of Use 00851906007040
Package 10851906007252
Package 20851906007259

Customer Contacts

Phone
18009310882