FDA UDI In Commercial Distribution 🇺🇸 United States

Continuum® Trilogy® Allofit® Vivacit-E®

DI: 00889024155367 · Model: 00-8851-021-36 · Zimmer, Inc.
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Continuum® Trilogy® Allofit® Vivacit-E®
Primary DI
00889024155367
Version / Model
00-8851-021-36
Catalog Number
00-8851-021-36
Company Name
Zimmer, Inc.
Labeler DUNS
056038268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
4
Public Version Date
2020-06-15
Public Version Status
Update
Public Device Record Key
2a753160-f508-4380-8afb-2451bb165b63

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
OQI Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
OQG Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented
OQH Hip, semi-constrained, cemented, metal/polymer + additive, cemented
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 00889024155367

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K120370 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 36 Millimeter
Device Size Text, specify Size TT