FDA UDI In Commercial Distribution 🇺🇸 United States

Discovery

DI: 00840682139373 · Model: NMCT 670 PRO · G E MEDICAL SYSTEMS ISRAEL LTD.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Discovery
Primary DI
00840682139373
Version / Model
NMCT 670 PRO
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
2018-05-15
Public Version
3
Public Version Date
2022-05-17
Public Version Status
Update
Public Device Record Key
4df75fe7-1a1d-4efe-ba8e-4d9b10616bc1

Device Description

D670 PRO NM GANTRY FINAL - NEW ROTOR

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

GMDN Terms

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

Identifiers

Type ID
Primary 00840682139373

Premarket Submissions

Submission Number Supplement Number
K093514 000