FDA UDI In Commercial Distribution 🇺🇸 United States

CrossFlow

DI: 07613327261035 · Model: 0450000125 · STRYKER CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
CrossFlow
Primary DI
07613327261035
Version / Model
0450000125
Catalog Number
0450-000-125
Company Name
STRYKER CORPORATION
Labeler DUNS
187502109
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
5
Public Version Date
2019-04-23
Public Version Status
Update
Public Device Record Key
455291ad-dc21-4435-9fb7-fc0b9e94791f

Device Description

Patient-Use Tubing, Do not use if package is damaged

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
47625 Surgical irrigation/aspiration tubing set

Identifiers

Type ID
Package 37613327261036
Primary 07613327261035

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K151932 000