FDA UDI In Commercial Distribution 🇺🇸 United States

NAUTILUS

DI: 08053307590196 · Model: NAUTILUS · TECHNIX SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
NAUTILUS
Primary DI
08053307590196
Version / Model
NAUTILUS
Company Name
TECHNIX SPA
Labeler DUNS
437977127
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-11-06
Public Version
1
Public Version Date
2024-11-14
Public Version Status
New
Public Device Record Key
f861a629-d3be-4c90-a103-d2238467362d

Device Description

Fixed equipment for radioscopy and radiography Brand: Dornier MedTech America, Inc

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
JAA System, X-Ray, Fluoroscopic, Image-Intensified

GMDN Terms

Code Name
37679 Stationary general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 08053307590196

Premarket Submissions

Submission Number Supplement Number
K220871 000