FDA UDI In Commercial Distribution 🇺🇸 United States

Flex

DI: 00851906007149 · Model: Box of Flex 12 count (English only) · The Flex Company
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
12

Basic Information

Brand Name
Flex
Primary DI
00851906007149
Version / Model
Box of Flex 12 count (English only)
Company Name
The Flex Company
Labeler DUNS
080314616
Distribution Status
In Commercial Distribution
Device Count in Pkg
12
Record Status
Published
Publish Date
2018-10-16
Public Version
4
Public Version Date
2022-09-02
Public Version Status
Update
Public Device Record Key
4776c5fe-3e2c-4372-92ce-96661ec2ac15

Device Description

Box of Flex Disc 12 count (Direct-to-Consumer)

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 00851906007149
Unit of Use 00851906007040
Package 10851906007146

Customer Contacts

Phone
18009310882