FDA UDI In Commercial Distribution 🇺🇸 United States

TRIMAX 3543 Detector

DI: 60889974160185 · Model: DETECTOR,PACKED,TRIMAX,3543 · CARESTREAM HEALTH, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TRIMAX 3543 Detector
Primary DI
60889974160185
Version / Model
DETECTOR,PACKED,TRIMAX,3543
Catalog Number
AE4200
Company Name
CARESTREAM HEALTH, INC.
Labeler DUNS
793169512
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-23
Public Version
5
Public Version Date
2019-05-07
Public Version Status
Update
Public Device Record Key
4751d871-f704-4fb7-a583-5ea1c4b83e64

Device Description

DETECTOR,PACKED,TRIMAX,3543

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
MQB Solid state x-ray imager (flat panel/digital imager)

GMDN Terms

Code Name
61108 Indirect flat panel x-ray detector

Identifiers

Type ID
Primary 60889974160185

Premarket Submissions

Submission Number Supplement Number
K150766 000