FDA UDI In Commercial Distribution 🇺🇸 United States

CombiDiagnost R90

DI: 00884838076747 · Model: 9890-010-70141 · Philips Medical Systems DMC GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
CombiDiagnost R90
Primary DI
00884838076747
Version / Model
9890-010-70141
Catalog Number
709030
Company Name
Philips Medical Systems DMC GmbH
Labeler DUNS
314101218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-09
Public Version
3
Public Version Date
2021-10-11
Public Version Status
Update
Public Device Record Key
91178961-637b-4d36-9051-9bf30c2926bb

Device Description

Image-intensified fluoroscopic x-ray system

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
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
No
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
37645 Stationary basic diagnostic x-ray system, digital

Identifiers

Type ID
Primary 00884838076747

Customer Contacts