FDA UDI In Commercial Distribution 🇺🇸 United States

INSTRUMENT

DI: 07613327000481 · Model: 6543-5-202 · Howmedica Osteonics Corp.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INSTRUMENT
Primary DI
07613327000481
Version / Model
6543-5-202
Catalog Number
6543-5-202
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-11-13
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
efedaf54-c467-4066-8484-16caea77e173

Device Description

TRIATHLON REVISION INSTRUMENTS TIBIAL CONE REAMER GUIDE

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
Yes
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
HTO REAMER

GMDN Terms

Code Name
45109 Orthopaedic reamer guide

Identifiers

Type ID
Primary 07613327000481

Device Sizes

Type Value Unit Text
Device Size Text, specify Side: Right Medial/Left Lateral