FDA UDI In Commercial Distribution 🇺🇸 United States

Trident II

DI: 07613327343915 · Model: 702-04-52E · Howmedica Osteonics Corp.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trident II
Primary DI
07613327343915
Version / Model
702-04-52E
Catalog Number
702-04-52E
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-20
Public Version
4
Public Version Date
2022-08-02
Public Version Status
Update
Public Device Record Key
28b20f6c-45ca-48c9-9a5b-ea3bbbf45150

Device Description

TRIDENT II TRITANIUM CLUSTER 52E

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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate
LZO Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 07613327343915

Device Sizes

Type Value Unit Text
Device Size Text, specify Alpha Code: E
Outer Diameter 52.0 Millimeter
Device Size Text, specify Number of Screw Holes: 5.0 Holes