FDA UDI In Commercial Distribution 🇺🇸 United States

DRI-LOK

DI: 07613327055757 · Model: 3910090500 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
DRI-LOK
Primary DI
07613327055757
Version / Model
3910090500
Catalog Number
3910-090-500
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-08-10
Public Version
1
Public Version Date
2020-08-18
Public Version Status
New
Public Device Record Key
587e21e6-c9ea-456d-bd11-043e497dfa67

Device Description

[Threaded Cannula. Do not resterilize, Do not use if package is damaged]

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
NBH Accessories, arthroscopic

GMDN Terms

Code Name
58752 Arthroscopic access cannula, single-use

Identifiers

Type ID
Package 37613327055758
Primary 07613327055757

Customer Contacts

Device Sizes

Type Value Unit Text
Length 90.0 Millimeter
Outer Diameter 5.0 Millimeter