FDA UDI In Commercial Distribution 🇺🇸 United States

EXTRON 3

DI: 08800018422601 · Model: EXTRON 3 · DRTECH Corporation
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
EXTRON 3
Primary DI
08800018422601
Version / Model
EXTRON 3
Company Name
DRTECH Corporation
Labeler DUNS
689842626
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-06-17
Public Version
1
Public Version Date
2025-06-25
Public Version Status
New
Public Device Record Key
d65ae13d-33f4-49c5-81a4-945d6ae96816

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
MR Unsafe
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
OXO Image-Intensified Fluoroscopic X-Ray System, Mobile
JAA System, X-Ray, Fluoroscopic, Image-Intensified
OWB Interventional Fluoroscopic X-Ray System

GMDN Terms

Code Name
37646 Mobile general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 08800018422601

Premarket Submissions

Submission Number Supplement Number
K250010 000