FDA UDI In Commercial Distribution 🇺🇸 United States

DUNLEE

DI: 00884838130609 · Model: 3T HD T/R KNEE ARRAY · Philips Medical Systems Nederland B.V.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DUNLEE
Primary DI
00884838130609
Version / Model
3T HD T/R KNEE ARRAY
Catalog Number
300007306912
Company Name
Philips Medical Systems Nederland B.V.
Labeler DUNS
413819707
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-03
Public Version
1
Public Version Date
2026-04-13
Public Version Status
New
Public Device Record Key
9d260bf4-e833-4e96-8000-2f1befd8b89e

Device Description

3T HD T/R KNEE ARRAY

Device Characteristics

Single Use
Yes
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
MOS Coil, Magnetic Resonance, Specialty

GMDN Terms

Code Name
40749 MRI system coil, radio-frequency

Identifiers

Type ID
Primary 00884838130609

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 65 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
10 – 100 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
50 – 106 KiloPascal