FDA UDI In Commercial Distribution 🇺🇸 United States

Vive

DI: 00810041987761 · Model: SUP2091BLK · 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
00810041987761
Version / Model
SUP2091BLK
Company Name
VIVE HEALTH LLC
Labeler DUNS
047025993
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-10
Public Version
1
Public Version Date
2024-06-18
Public Version Status
New
Public Device Record Key
c7db08fb-6b86-43a3-a0ea-bec5c4d2bf38

Device Description

Dual Trigger FInger Splint

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
ILH Splint, Hand, And Components

GMDN Terms

Code Name
42874 Hand/finger splint, reusable

Identifiers

Type ID
Primary 00810041987761
Package 10810041987768