FDA UDI In Commercial Distribution 🇺🇸 United States

TroFlex

DI: 07613252645894 · Model: 0306011500 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
TroFlex
Primary DI
07613252645894
Version / Model
0306011500
Catalog Number
0306011500
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
1
Public Version Date
2018-10-25
Public Version Status
New
Public Device Record Key
92a241b5-fd06-4e86-b0b2-bd43904f0a95

Device Description

Curved Needle

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OAR Injector, vertebroplasty (does not contain cement)

GMDN Terms

Code Name
47737 Orthopaedic cement injection cannula

Identifiers

Type ID
Package 37613252645895
Primary 07613252645894

Customer Contacts