FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613154598991 · Model: 5920000003 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613154598991
Version / Model
5920000003
Catalog Number
5920-000-003
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-09-22
Public Version
4
Public Version Date
2023-06-21
Public Version Status
Update
Public Device Record Key
2da484ab-b0d2-48b0-985a-b78fa38aaa9e

Device Description

Sterile Tubing Extension, Single, Luer Lock

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
KCY TOURNIQUET, PNEUMATIC

GMDN Terms

Code Name
14074 Surgical pneumatic tourniquet system

Identifiers

Type ID
Package 37613154598992
Primary 07613154598991

Customer Contacts

Device Sizes

Type Value Unit Text
Length 60.0 Inch