FDA UDI In Commercial Distribution 🇺🇸 United States

E-ST

DI: 00815871020428 · Model: 60132PRO2 · Avante
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
E-ST
Primary DI
00815871020428
Version / Model
60132PRO2
Company Name
Avante
Labeler DUNS
178440426
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
4
Public Version Date
2019-06-19
Public Version Status
Update
Public Device Record Key
ecbefd75-15c1-4074-84c2-ebc6abfe45bd

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
HEP Monitor, Blood-Flow, Ultrasonic
KNG Monitor, Ultrasonic, Fetal

GMDN Terms

Code Name
40761 General-purpose ultrasound imaging system

Identifiers

Type ID
Primary 00815871020428

Customer Contacts

Phone
502-244-4444