FDA UDI In Commercial Distribution 🇺🇸 United States

SureEase Ultra 3

DI: 00852598007264 · Model: Constriction Ring · AUGUSTA MEDICAL SYSTEMS, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SureEase Ultra 3
Primary DI
00852598007264
Version / Model
Constriction Ring
Company Name
AUGUSTA MEDICAL SYSTEMS, L.L.C.
Labeler DUNS
052255606
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-17
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
ac8218ec-1d97-4a87-9aae-7cdfd6378f54

Device Description

Constriction Ring

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LKY Device, External Penile Rigidity

GMDN Terms

Code Name
17744 Penile vacuum device

Identifiers

Type ID
Primary 00852598007264

Customer Contacts

Phone
800-827-8382