FDA UDI Not in Commercial Distribution 🇺🇸 United States

La Vie

DI: 00036000512083 · Model: Pad · KIMBERLY-CLARK GLOBAL SALES, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
48

Basic Information

Brand Name
La Vie
Primary DI
00036000512083
Version / Model
Pad
Company Name
KIMBERLY-CLARK GLOBAL SALES, INC.
Labeler DUNS
829568273
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
48
Record Status
Published
Publish Date
2020-07-01
Public Version
3
Public Version Date
2021-09-30
Public Version Status
Update
Public Device Record Key
9b6e06be-94e0-4f05-baf7-e3aa5d0135b5
Distribution End Date
2021-09-30

Device Description

LA VIE OVERNIGHT WINGED PAD 48

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HHD Pad, menstrual, unscented

GMDN Terms

Code Name
40545 Menstrual pad, unscented

Identifiers

Type ID
Unit of Use 00036000536799
Primary 00036000512083

Customer Contacts