FDA UDI In Commercial Distribution 🇺🇸 United States

Dr. Joel Kaplan

DI: 00850005747567 · Model: 0302-225-W · Dr. Joel Kaplan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Dr. Joel Kaplan
Primary DI
00850005747567
Version / Model
0302-225-W
Company Name
Dr. Joel Kaplan, Inc.
Labeler DUNS
003934314
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-04-14
Public Version
1
Public Version Date
2025-04-22
Public Version Status
New
Public Device Record Key
9b47d769-43b0-4d63-8166-3c3394326256

Device Description

Metal Hand Pump System - Size Large

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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 00850005747567

Customer Contacts

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 2.25 Inch
Length 9 Inch