FDA UDI Not in Commercial Distribution 🇺🇸 United States

Invivo

DI: 00884838081765 · Model: 4535-302-23311 · Philips DS North America LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Invivo
Primary DI
00884838081765
Version / Model
4535-302-23311
Catalog Number
989603111532
Company Name
Philips DS North America LLC
Labeler DUNS
118983916
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-04-17
Public Version
8
Public Version Date
2024-02-12
Public Version Status
Update
Public Device Record Key
c61a5dbd-e902-4c38-b5fc-bb8079b9805c
Distribution End Date
2021-12-15

Device Description

Baseplate Assembly, Prostate, SMS

Device Characteristics

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GDF GUIDE, NEEDLE, SURGICAL

GMDN Terms

Code Name
60734 Needle guide, reusable

Identifiers

Type ID
Primary 00884838081765

Customer Contacts

Storage Conditions

Type
Storage Environment Humidity
Temperature Range
5 – 95 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
70 – 110 KiloPascal
Type
Storage Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius