FDA UDI In Commercial Distribution 🇺🇸 United States

DuraDiagnost

DI: 00884838095205 · Model: 712203 · Philips Healthcare (Suzhou) Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DuraDiagnost
Primary DI
00884838095205
Version / Model
712203
Company Name
Philips Healthcare (Suzhou) Co., Ltd.
Labeler DUNS
421265537
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-04
Public Version
3
Public Version Date
2023-07-17
Public Version Status
Update
Public Device Record Key
0597d8d6-7af7-484e-875d-034c4e64d481

Device Description

Stationary x-ray 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
No
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 00884838095205

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K201640 000

Storage Conditions

Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Handling Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
18 – 30 Degrees Celsius
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Humidity
Temperature Range
10 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-10 – 55 Degrees Celsius