FDA UDI In Commercial Distribution 🇺🇸 United States

INSTRUMENT

DI: 07613327363531 · Model: 7002-0157 · Howmedica Osteonics Corp.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INSTRUMENT
Primary DI
07613327363531
Version / Model
7002-0157
Catalog Number
7002-0157
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-01
Public Version
6
Public Version Date
2022-12-14
Public Version Status
Update
Public Device Record Key
fc7343af-fcb6-4d07-abd9-5a85fcf6d74d

Device Description

TRIDENT II WINDOW TRIAL

Device Characteristics

Single Use
No
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
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MEH Prosthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
KWZ Prosthesis, hip, constrained, cemented or uncemented, metal/polymer
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
58480 Acetabulum prosthesis trial, prefabricated, reusable

Identifiers

Type ID
Primary 07613327363531

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 57.0 Millimeter