FDA UDI In Commercial Distribution 🇺🇸 United States

ELI Edit

DI: 00817655022802 · Model: 11049-011-51 · MORTARA INSTRUMENT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ELI Edit
Primary DI
00817655022802
Version / Model
11049-011-51
Company Name
MORTARA INSTRUMENT, INC.
Labeler DUNS
062046149
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-13
Public Version
4
Public Version Date
2020-06-29
Public Version Status
Update
Public Device Record Key
830be1d8-1fb1-4704-9890-3a56d51f3345

Device Description

Cardiology Data Software

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DPS Electrocardiograph

GMDN Terms

Code Name
38473 Patient health record information system

Identifiers

Type ID
Primary 00817655022802

Customer Contacts

Phone
888-667-8272

Premarket Submissions

Submission Number Supplement Number
K930558 000