FDA UDI Not in Commercial Distribution 🇺🇸 United States

Color Cuff

DI: 07613154600182 · Model: 5922218136 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Color Cuff
Primary DI
07613154600182
Version / Model
5922218136
Catalog Number
5922-218-136
Company Name
STRYKER CORPORATION
Labeler DUNS
196548481
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
4
Public Version Date
2021-12-31
Public Version Status
Update
Public Device Record Key
332924bb-6d90-40b5-9da1-0883c22ceec9
Distribution End Date
2021-12-31

Device Description

Non-Sterile Reusable Tourniquet Cuff Single Bladder, Single Port and Luer Lock Connector

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
No

Product Codes

Code Name
KCY TOURNIQUET, PNEUMATIC

GMDN Terms

Code Name
17230 Tourniquet cuff, reusable

Identifiers

Type ID
Primary 07613154600182

Customer Contacts

Device Sizes

Type Value Unit Text
Width 4.0 Inch
Length 18.0 Inch