FDA UDI In Commercial Distribution 🇺🇸 United States

VEGA System® PS

DI: 04046964452048 · Model: NX351 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
VEGA System® PS
Primary DI
04046964452048
Version / Model
NX351
Catalog Number
NX351
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-11-11
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
3dd671e8-1f3b-43ce-b0d8-6370e94fd578

Device Description

ALL POLY TIBIA VEGA PS T5 12MM

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

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
33665 Posterior-stabilized total knee prosthesis

Identifiers

Type ID
Primary 04046964452048

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Figure / Size : T5
Device Size Text, specify Implant Fixation : cemented