FDA UDI In Commercial Distribution 🇺🇸 United States

STAR

DI: 00886385017105 · Model: 903-0053 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STAR
Primary DI
00886385017105
Version / Model
903-0053
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-27
Public Version
3
Public Version Date
2022-05-16
Public Version Status
Update
Public Device Record Key
29a106d8-94c7-4575-8364-5c6647a92289

Device Description

KEEL BROACH

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
NTG Prosthesis, Ankle, Uncemented, Non-Constrained

GMDN Terms

Code Name
36167 Orthopaedic broach

Identifiers

Type ID
Primary 00886385017105

Customer Contacts