FDA UDI In Commercial Distribution 🇺🇸 United States

Sentinelle

DI: 00884838103740 · Model: 459801813441 · Philips Ds North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sentinelle
Primary DI
00884838103740
Version / Model
459801813441
Company Name
Philips Ds North America LLC
Labeler DUNS
009237140
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-02-24
Public Version
4
Public Version Date
2024-02-16
Public Version Status
Update
Public Device Record Key
b63bf318-01e3-482d-8c89-200d16d59536

Device Description

Sentinelle, Biopsy Grid

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
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

Identifiers

Type ID
Primary 00884838103740
Package 10884838103747

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius
Type
Handling Environment Temperature
Temperature Range
10 – 24 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 90 Percent (%) Relative Humidity