FDA UDI Not in Commercial Distribution 🇺🇸 United States

PROSA

DI: 04041906142247 · Model: FV812T · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROSA
Primary DI
04041906142247
Version / Model
FV812T
Catalog Number
FV812T
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-05-21
Public Version
3
Public Version Date
2021-05-07
Public Version Status
Update
Public Device Record Key
279b25ba-5dd3-4a1e-acc8-9e694e0c9837
Distribution End Date
2021-03-11

Device Description

PROSA SYS MININAV 0 & PED.SPRUNG RES.

Device Characteristics

Single Use
Yes
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
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JXG Shunt, central nervous system and components

GMDN Terms

Code Name
61123 Ventriculo-peritoneal/atrial shunt

Identifiers

Type ID
Primary 04041906142247

Customer Contacts