FDA UDI In Commercial Distribution 🇺🇸 United States

NA

DI: 07613154615513 · Model: 5920000309 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
NA
Primary DI
07613154615513
Version / Model
5920000309
Catalog Number
5920-000-309
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
2023-06-21
Public Version Status
Update
Public Device Record Key
a17dc416-53c7-401b-9d64-03698df3f37e

Device Description

Non-Sterile Adapter, Single, 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 37613154615514
Primary 07613154615513

Customer Contacts