FDA UDI In Commercial Distribution 🇺🇸 United States

Philips

DI: 00884838118775 · Model: 989603207293 · Philips Medical Systems Nederland B.V.
Product Codes
1
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Philips
Primary DI
00884838118775
Version / Model
989603207293
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
2024-07-18
Public Version
1
Public Version Date
2024-07-26
Public Version Status
New
Public Device Record Key
069645ba-5261-46ef-8e66-a480d1c1b692

Device Description

Kit, Enhanced Access, Bilateral Upgrade consists of Fiducial Marker Grid Block Assembly; 3 Grid Plate Enhanced Access, Lateral; 3 Grid Plate, Enhanced Access Medial; 2 IMMOBILIZATION SYSTEM, M/L, LBS ENHANCED; MRI Needle Block 12G; MRI Needle Block 14G; MRI Needle Block 18G; 2 Needle Block Holder; MRI Needle Block 16G.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
Yes
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PXP Breast Biopsy / Localization Tray

GMDN Terms

Code Name
45018 Needle guide, single-use
60734 Needle guide, reusable

Identifiers

Type ID
Primary 00884838118775

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius