FDA UDI In Commercial Distribution 🇺🇸 United States

E-ST

DI: 00815871020381 · Model: 601324 · Avante
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
E-ST
Primary DI
00815871020381
Version / Model
601324
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
03698ef9-67d4-4181-ac5a-052856672ac2

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
KNG Monitor, Ultrasonic, Fetal
HEP Monitor, Blood-Flow, Ultrasonic

GMDN Terms

Code Name
40761 General-purpose ultrasound imaging system

Identifiers

Type ID
Primary 00815871020381

Customer Contacts

Phone
502-244-4444