FDA UDI In Commercial Distribution 🇺🇸 United States

Invivo

DI: 00884838083615 · Model: 98960321422 · Philips Ds North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Invivo
Primary DI
00884838083615
Version / Model
98960321422
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
2016-09-23
Public Version
9
Public Version Date
2023-07-10
Public Version Status
Update
Public Device Record Key
98d2d8d2-e2fd-4f35-830c-e91b786d305e

Device Description

Biopsy Grid (User-sterilized)

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
MR Conditional
Direct Marking Exempt
Yes
PM Exempt
No
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
Yes
Sterilization Methods
["Moist Heat or Steam Sterilization", "Liquid Chemical"]

Product Codes

Code Name
MOS Coil, magnetic resonance, specialty

GMDN Terms

Code Name
40749 MRI system coil, radio-frequency

Identifiers

Type ID
Primary 00884838083615

Customer Contacts

Storage Conditions

Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal
Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
30 – 75 Percent (%) Relative Humidity
Type
Handling Environment Temperature
Temperature Range
10 – 24 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
30 – 90 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
70 – 106 KiloPascal