FDA UDI In Commercial Distribution 🇺🇸 United States

Invivo

DI: 00884838067301 · Model: 98960301016 · Philips Ds North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Invivo
Primary DI
00884838067301
Version / Model
98960301016
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
6
Public Version Date
2023-07-10
Public Version Status
Update
Public Device Record Key
cbb45cb5-a2c4-4d6b-b926-de76aa7effbe

Device Description

Quadrature Knee/Foot Coil

Device Characteristics

Single Use
No
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 Safe
Direct Marking Exempt
Yes
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
LNH System, nuclear magnetic resonance imaging

GMDN Terms

Code Name
40749 MRI system coil, radio-frequency

Identifiers

Type ID
Primary 00884838067301

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity