FDA UDI In Commercial Distribution 🇺🇸 United States

Encore

DI: 00850358007165 · Model: INSPECTED PREMIUM MANUAL PUMP U.S. · ENCORE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Encore
Primary DI
00850358007165
Version / Model
INSPECTED PREMIUM MANUAL PUMP U.S.
Catalog Number
1101-PREMIUM
Company Name
ENCORE, INC.
Labeler DUNS
614647725
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-07-25
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
280a197d-be94-4834-a5ce-a9e10a823f4e

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
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
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 00850358007165

Customer Contacts

Phone
800-475-3091