FDA UDI In Commercial Distribution 🇺🇸 United States

Invivo

DI: 00884838073159 · Model: 98960320913 · Philips Ds North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Invivo
Primary DI
00884838073159
Version / Model
98960320913
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
2024-02-16
Public Version Status
Update
Public Device Record Key
e94df2cf-a5e2-4b9b-8349-6af9d408ec0e

Device Description

Grid Plate, Enhanced Access, lat.

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GDF GUIDE, NEEDLE, SURGICAL

GMDN Terms

Code Name
45018 Needle guide, single-use

Identifiers

Type ID
Primary 00884838073159

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