FDA UDI In Commercial Distribution 🇺🇸 United States

RINGFIX

DI: 00886385010205 · Model: 451-2015 · Stryker Trauma SA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
RINGFIX
Primary DI
00886385010205
Version / Model
451-2015
Catalog Number
451-2015
Company Name
Stryker Trauma SA
Labeler DUNS
481999654
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
3
Public Version Date
2018-11-22
Public Version Status
Update
Public Device Record Key
2cb857b9-c915-4b1f-b88d-5c5ded9dbf06

Device Description

K-Wire, DLC

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

Product Codes

Code Name
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
32390 Fluted surgical drill bit, reusable

Identifiers

Type ID
Primary 00886385010205

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 1.8 Millimeter
Length 400.0 Millimeter