FDA UDI In Commercial Distribution 🇺🇸 United States

Vector Base

DI: 00815962020283 · Model: VEC-3000 · BIONESS INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vector Base
Primary DI
00815962020283
Version / Model
VEC-3000
Company Name
BIONESS INC.
Labeler DUNS
182287727
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-07
Public Version
3
Public Version Date
2020-05-20
Public Version Status
Update
Public Device Record Key
768c7658-1043-40f7-ab26-95d55ebf4e54

Device Description

Vector Gait and Safety System, Base Model

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
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
Yes
Has Serial Number
Yes
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
64812 Gait rehabilitation frame, manual

Identifiers

Type ID
Primary 00815962020283

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius