FDA UDI In Commercial Distribution 🇺🇸 United States

ICONIX

DI: 07613252450467 · Model: 3910-500-561 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ICONIX
Primary DI
07613252450467
Version / Model
3910-500-561
Catalog Number
3910-500-561
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-04
Public Version
4
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
1da3dfac-0d77-4b16-92e3-090e4800e88c

Device Description

2.3MM ICONIX 25¿ SLANT 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
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
35095 Surgical drill guide, reusable

Identifiers

Type ID
Primary 07613252450467

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 2.3 Millimeter
Angle 25.0 degree