FDA UDI In Commercial Distribution 🇺🇸 United States

RevoluX

DI: 04719892352000 · Model: NDR705 · NANORAY BIOTECH CO., LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RevoluX
Primary DI
04719892352000
Version / Model
NDR705
Company Name
NANORAY BIOTECH CO., LTD.
Labeler DUNS
658696687
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-11-02
Public Version
1
Public Version Date
2023-11-10
Public Version Status
New
Public Device Record Key
1fee3fee-16ec-46c5-bd2e-0d8c25abe6ba

Device Description

Hand Diagnostic Radiography Imaging System

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
Yes
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
KPR System, X-Ray, Stationary

GMDN Terms

Code Name
37645 Stationary basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 04719892352000

Customer Contacts

Phone
+88627968909

Premarket Submissions

Submission Number Supplement Number
K220271 000