FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 34546540756979 · Model: 234-500-227 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
NA
Primary DI
34546540756979
Version / Model
234-500-227
Catalog Number
234-500-227
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2015-09-04
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
a70e1f65-8af2-40fd-b6b1-2bd3d4fae0f2

Device Description

.027" CROSS-SCREW FLEXIBLE CANNULA WITH SLEEVES

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
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", "Ethylene Oxide"]

Product Codes

Code Name
NBH ACCESSORIES,ARTHROSCOPIC

GMDN Terms

Code Name
58148 Orthopaedic implantation sleeve, single-use

Identifiers

Type ID
Primary 34546540756979
Unit of Use 04546540756978

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Diameter: 0.027 Inch