FDA UDI In Commercial Distribution 🇺🇸 United States

Dri-Lok

DI: 07613327061109 · Model: 3910090006 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Dri-Lok
Primary DI
07613327061109
Version / Model
3910090006
Catalog Number
3910-090-006
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-07-14
Public Version
1
Public Version Date
2020-07-22
Public Version Status
New
Public Device Record Key
a68c4df2-09d6-4449-9bbc-dc84c7587d3b

Device Description

Cannulated Obturator Assembly for Use with 8.0 mm x 90 mm Dri-Lok Cannula Obturator

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
35692 Rigid endoscope obturator

Identifiers

Type ID
Primary 07613327061109

Customer Contacts