FDA UDI In Commercial Distribution 🇺🇸 United States

DURAY

DI: 00990010301283 · Model: XR2012 · Beyes Dental Canada Inc
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DURAY
Primary DI
00990010301283
Version / Model
XR2012
Catalog Number
DURAY V2
Company Name
Beyes Dental Canada Inc
Labeler DUNS
244261462
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-05-11
Public Version
1
Public Version Date
2023-05-19
Public Version Status
New
Public Device Record Key
971c1d56-fbe0-4b25-972d-dd202014f2c7

Device Description

DURAY V2, MOBILE DC Intraoral X-Ray, 60kV & 70kV, 100-230V, 50/60 Hz, 80cm arm length

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
MR Safe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
EHD Unit, X-Ray, Extraoral With Timer

GMDN Terms

Code Name
42297 Stationary intraoral dental x-ray system, digital

Identifiers

Type ID
Primary 00990010301283

Premarket Submissions

Submission Number Supplement Number
K031118 000