FDA UDI In Commercial Distribution 🇺🇸 United States

Vive

DI: 00810041983107 · Model: SUP2059BLKL · VIVE HEALTH LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Vive
Primary DI
00810041983107
Version / Model
SUP2059BLKL
Company Name
VIVE HEALTH LLC
Labeler DUNS
047025993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-05
Public Version
1
Public Version Date
2024-06-13
Public Version Status
New
Public Device Record Key
74f17278-9e55-4a78-8d2e-e6a674a76c76

Device Description

Cross Support Back Brace (Large)

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
IQE Orthosis, Lumbar

GMDN Terms

Code Name
33031 Lumbar spine orthosis

Identifiers

Type ID
Package 10810041983104
Primary 00810041983107