FDA UDI Not in Commercial Distribution 🇺🇸 United States

STAR™

DI: 00886385018102 · Model: 925-0016 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
STAR™
Primary DI
00886385018102
Version / Model
925-0016
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-06-27
Public Version
5
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
ff839874-2020-4bc1-abfb-78058f4da2a2
Distribution End Date
2014-11-07

Device Description

ANTERTIOR CHAMFER REAMER, 7.5mm

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
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Primary 00886385018102

Customer Contacts

Device Sizes

Type Value Unit Text
Outer Diameter 7.5 Millimeter