FDA UDI In Commercial Distribution 🇺🇸 United States

Vive

DI: 00810178883912 · Model: LVA3106BLUM · VIVE HEALTH LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vive
Primary DI
00810178883912
Version / Model
LVA3106BLUM
Company Name
VIVE HEALTH LLC
Labeler DUNS
047025993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-08-07
Public Version
1
Public Version Date
2025-08-15
Public Version Status
New
Public Device Record Key
00c3f95c-6876-40c7-a0c2-8fc9d3024104

Device Description

Patient Lift Toilet Sling (Medium)

Device Characteristics

Single Use
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IKX Aid, Transfer

GMDN Terms

Code Name
66996 Patient transfer/turning sheet, reusable

Identifiers

Type ID
Primary 00810178883912