FDA UDI In Commercial Distribution 🇺🇸 United States

O-ARM®

DI: 00763000355555 · Model: BI70002000 · MEDTRONIC NAVIGATION, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
O-ARM®
Primary DI
00763000355555
Version / Model
BI70002000
Company Name
MEDTRONIC NAVIGATION, INC.
Labeler DUNS
803580559
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-10-16
Public Version
1
Public Version Date
2020-10-26
Public Version Status
New
Public Device Record Key
a5448d8c-28eb-41a5-b6b0-243a989678cf

Device Description

O-ARM SYS BI70002000 O2 UE 120V B EN UEN

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
OXO Image-intensified fluoroscopic x-ray system, mobile
OWB Interventional fluoroscopic x-ray system

GMDN Terms

Code Name
37649 Portable general-purpose fluoroscopic x-ray system, digital

Identifiers

Type ID
Primary 00763000355555

Customer Contacts