FDA UDI In Commercial Distribution 🇺🇸 United States

Vivacit-E®

DI: 00889024572829 · Model: 110031314 · Zimmer, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vivacit-E®
Primary DI
00889024572829
Version / Model
110031314
Catalog Number
110031314
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-31
Public Version
1
Public Version Date
2020-01-08
Public Version Status
New
Public Device Record Key
81d4fd53-1a9c-43bf-bc30-483516702c18

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
MR Conditional
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
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
KWY Prosthesis, hip, hemi-, femoral, metal/polymer, cemented or uncemented

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 00889024572829

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K190656 000

Device Sizes

Type Value Unit Text
Outer Diameter 36.00 Millimeter
Lumen/Inner Diameter 22.20 Millimeter
Device Size Text, specify Size B