FDA UDI In Commercial Distribution 🇺🇸 United States

Flex

DI: 00850037498147 · Model: 10035 · The Flex Company
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
16

Basic Information

Brand Name
Flex
Primary DI
00850037498147
Version / Model
10035
Company Name
The Flex Company
Labeler DUNS
080314616
Distribution Status
In Commercial Distribution
Device Count in Pkg
16
Record Status
Published
Publish Date
2023-01-06
Public Version
1
Public Version Date
2023-01-16
Public Version Status
New
Public Device Record Key
85c1790b-fffc-49f2-92db-ab757a8a734d

Device Description

Flex Disc 16ct Bag

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
Yes
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
Yes
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
Package 10850037498144
Primary 00850037498147
Unit of Use 00851906007040

Customer Contacts

Phone
18009310882