FDA UDI In Commercial Distribution 🇺🇸 United States

Trident

DI: 07613327037814 · Model: 621-10-32F · Howmedica Osteonics Corp.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Trident
Primary DI
07613327037814
Version / Model
621-10-32F
Catalog Number
621-10-32F
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2021-12-28
Public Version Status
Update
Public Device Record Key
38611a82-0739-4808-958c-093c600e7777

Device Description

10 Degree Polyethylene Insert

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
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
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
43168 Non-constrained polyethylene acetabular liner

Identifiers

Type ID
Primary 07613327037814

Premarket Submissions

Submission Number Supplement Number
K983382 000
K983502 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Alpha Code: F
Lumen/Inner Diameter 32.0 Millimeter