FDA UDI Not in Commercial Distribution 🇺🇸 United States

VERASENSE

DI: 00816818020600 · Model: VERASENSE for Biomet Vanguard PS size 63/67 · ORTHOSENSOR INC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VERASENSE
Primary DI
00816818020600
Version / Model
VERASENSE for Biomet Vanguard PS size 63/67
Catalog Number
BMT-VGPS 63
Company Name
ORTHOSENSOR INC
Labeler DUNS
005788130
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-04-21
Public Version
8
Public Version Date
2023-07-31
Public Version Status
Update
Public Device Record Key
f257cfb3-7bf8-48ab-a4b4-f1b6ae087041
Distribution End Date
2023-06-30

Device Characteristics

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
ONN Intraoperative Orthopedic Joint Assessment Aid

GMDN Terms

Code Name
58988 Arthroplasty force sensor

Identifiers

Type ID
Primary 00816818020600

Storage Conditions

Type
Handling Environment Humidity
Temperature Range
30 – 100 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
15 – 37 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
36 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 80 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
0 – 50 Degrees Celsius
Type
Handling Environment Atmospheric Pressure
Temperature Range
47 – 106 KiloPascal