FDA UDI In Commercial Distribution 🇺🇸 United States

NMCT 850

DI: 00198953061336 · Model: H3907BE, H3907BF · G E MEDICAL SYSTEMS ISRAEL LTD.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NMCT 850
Primary DI
00198953061336
Version / Model
H3907BE, H3907BF
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
2025-09-09
Public Version
2
Public Version Date
2026-01-30
Public Version Status
Update
Public Device Record Key
543a0136-b9c3-40a2-8dc5-a896c5d1bae9

Device Description

NM_CT 850 NM Gantry Final MDR

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
No
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
37618 Full-body CT system
40640 Stationary gamma camera system

Identifiers

Type ID
Primary 00198953061336

Premarket Submissions

Submission Number Supplement Number
K173816 000