FDA UDI In Commercial Distribution 🇺🇸 United States

FibroScan

DI: 03662264001031 · Model: FibroScan 502 Touch · ECHOSENS
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
FibroScan
Primary DI
03662264001031
Version / Model
FibroScan 502 Touch
Company Name
ECHOSENS
Labeler DUNS
571069108
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2020-03-11
Public Version Status
Update
Public Device Record Key
25caab36-640f-4c0a-b229-a1abd96d27a1

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
IYO System, Imaging, Pulsed Echo, Ultrasonic

GMDN Terms

Code Name
58710 Hepatic ultrasound elastography system

Identifiers

Type ID
Primary 03662264001031

Customer Contacts

Phone
+33149818929

Premarket Submissions

Submission Number Supplement Number
K123806 000
K150239 000
K150949 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 50 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 85 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
54 – 106 KiloPascal
Type
Handling Environment Temperature
Temperature Range
10 – 40 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal