Dr. Joel Kaplan

GUDID 00850005747550

Penile vacuum device

Primary Device ID	00850005747550
NIH Device Record Key	998caccc-d07c-46d3-a6f8-c1cdf04723d5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Dr. Joel Kaplan
Version Model Number	0302-200-W
Company DUNS	003934314
Company Name	Dr. Joel Kaplan, Inc.
Device Count	1
DM Exempt	false
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	true
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	false
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00850005747550 [Primary]

LKY	Device, External Penile Rigidity

Steralize Prior To Use	false
Device Is Sterile	false

00850005747574	Metal Hand Pump System - Size Extra Large
00850005747567	Metal Hand Pump System - Size Large
00850005747550	Metal Hand Pump System - Size Medium
00850005747543	Dr. Joel Kaplan Metal Hand Pump System - Size Small
00850005747291	9" x 2.50" Cylinder
00850005747284	9" x 2.25" Cylinder
00850005747277	9" x 2.00" Cylinder
00850005747260	9" x 1.75" Cylinder
00850005747079	Metal Hand Pump

Mark Image Registration \| Serial	Company Trademark Application Date
DR. JOEL KAPLAN 90635333 not registered Live/Pending	Kaplan, Barry Joel 2021-04-09
DR. JOEL KAPLAN 78399697 3298753 Dead/Cancelled	BARRY JOEL KAPLAN, INC. 2004-04-09
DR. JOEL KAPLAN 78399688 2943924 Live/Registered	BARRY JOEL KAPLAN 2004-04-09