FDA UDI In Commercial Distribution 🇺🇸 United States

870ES to 870 DR Upgrade

DI: 00840682145947 · Model: H3906EF · G E MEDICAL SYSTEMS ISRAEL LTD.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
870ES to 870 DR Upgrade
Primary DI
00840682145947
Version / Model
H3906EF
Company Name
G E MEDICAL SYSTEMS ISRAEL LTD.
Labeler DUNS
532102365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-06-18
Public Version
1
Public Version Date
2019-06-26
Public Version Status
New
Public Device Record Key
c551b652-56b4-4840-82c0-38f07ebef089

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
JAK System, x-ray, tomography, computed
KPS System, tomography, computed, emission

GMDN Terms

Code Name
40640 Stationary gamma camera system
37618 Full-body CT system

Identifiers

Type ID
Primary 00840682145947

Premarket Submissions

Submission Number Supplement Number
K093514 000