FDA UDI In Commercial Distribution 🇺🇸 United States

Sunmed

DI: 10889483005613 · Model: 7-6515-22 · SUNMED, LLC
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Sunmed
Primary DI
10889483005613
Version / Model
7-6515-22
Company Name
SUNMED, LLC
Labeler DUNS
069009268
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-05
Public Version
9
Public Version Date
2020-12-04
Public Version Status
Update
Public Device Record Key
def08b7c-89b5-41df-be93-20eade2b463a

Device Description

2 Way Foley Catheter 5cc Balloon 22fr

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
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
EZL Catheter, Retention Type, Balloon

GMDN Terms

Code Name
34917 Indwelling urethral drainage balloon catheter, non-antimicrobial

Identifiers

Type ID
Package 20889483005610
Primary 10889483005613

Customer Contacts

Phone
800-433-2797

Premarket Submissions

Submission Number Supplement Number
K082815 000

Device Sizes

Type Value Unit Text
Catheter Gauge 22 French

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
34917
Type
Handling Environment Temperature
Temperature Range
– 49 Degrees Celsius