FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613154599134 · Model: 5920000205 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613154599134
Version / Model
5920000205
Catalog Number
5920-000-205
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
3
Public Version Date
2023-06-20
Public Version Status
Update
Public Device Record Key
0fc1f983-8868-4a55-80b1-d56a0a6c0292

Device Description

Non-Sterile Fill Line, Set, Luer Lock to Quick Connect

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

Product Codes

Code Name
KCY TOURNIQUET, PNEUMATIC

GMDN Terms

Code Name
14074 Surgical pneumatic tourniquet system

Identifiers

Type ID
Package 37613154599135
Primary 07613154599134

Customer Contacts

Device Sizes

Type Value Unit Text
Length 10.0 Feet