FDA UDI In Commercial Distribution 🇺🇸 United States

Flex

DI: 00851906007071 · Model: Flex 8 count bag (English only) · The Flex Company
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
8

Basic Information

Brand Name
Flex
Primary DI
00851906007071
Version / Model
Flex 8 count bag (English only)
Company Name
The Flex Company
Labeler DUNS
080314616
Distribution Status
In Commercial Distribution
Device Count in Pkg
8
Record Status
Published
Publish Date
2018-06-20
Public Version
3
Public Version Date
2022-01-26
Public Version Status
Update
Public Device Record Key
8336b429-a96e-441a-a3b2-a23d6115b3d7

Device Description

Flex 8 count bag (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 00851906007071
Unit of Use 00851906007040
Package 20851906007051

Customer Contacts

Phone
18009310882