FDA UDI In Commercial Distribution 🇺🇸 United States

Livia

DI: 07290016952001 · Model: livia-lavender · LIFE CARE LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Livia
Primary DI
07290016952001
Version / Model
livia-lavender
Catalog Number
livia-lavender
Company Name
LIFE CARE LTD
Labeler DUNS
514603588
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-08-02
Public Version
1
Public Version Date
2023-08-10
Public Version Status
New
Public Device Record Key
a0534f74-c3bc-441d-b279-485a23793e76

Device Description

Livia - Menstrual Pain Relief Device (Full set with lavender Cover)

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
No
Has Serial Number
Yes
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
NUH Stimulator, Nerve, Transcutaneous, Over-The-Counter

GMDN Terms

Code Name
35372 Analgesic transcutaneous electrical nerve stimulation system

Identifiers

Type ID
Primary 07290016952001

Customer Contacts

Phone
+97299747479