Primary Device ID | 07540198000336 |
NIH Device Record Key | 4e00f720-babb-456d-9c07-e741eeec1113 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pro-Fit |
Version Model Number | Regular Speculum Pack with stop disc |
Catalog Number | 8115 |
Company DUNS | 250896255 |
Company Name | Prime Pacific Health Innovations Corporation |
Device Count | 20 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540198000336 [Primary] |
GS1 | 07540198000411 [Unit of Use] |
FFQ | Speculum, Rectal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-08-09 |
Device Publish Date | 2016-09-30 |
07540198001265 | The Pro-Fit Universal Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting |
07540198001203 | The Pro-Fit Small Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of a |
07540198001159 | The Pro-Fit Regular Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of |
07540198001104 | The Pro-Fit Small Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of a |
07540198001050 | The Pro-Fit Regular Kit is a Colon Hydrotherapy Disposable Single-Use Speculum Kit consisting of |
07540198000398 | The Pro-Fit Universal Speculum Pack is a package containing 20 individual Disposable, Single-use |
07540198000381 | The Pro-Fit Universal Speculum Pack is a package containing 10 individual Disposable, Single-use |
07540198000374 | The Pro-Fit Regular Speculum Pack is a package containing 20 individual Disposable, Single-use S |
07540198000367 | The Pro-Fit Regular Speculum Pack is a package containing 10 individual Disposable, Single-use S |
07540198000350 | The Pro-Fit Small Speculum Pack is a package containing 20 individual Disposable, Single-use Spe |
07540198000343 | The Pro-Fit Small Speculum Pack is a package containing 10 individual Disposable, Single-use Spe |
07540198000336 | The Pro-Fit Regular Speculum Pack is a package containing 20 individual Disposable, Single-use S |
07540198000329 | The Pro-Fit Regular Speculum Pack is a package containing 10 individual Disposable, Single-use S |
07540198000312 | The Pro-Fit Small Speculum Pack is a package containing 20 individual Disposable, Single-use Spe |
07540198000305 | The Pro-Fit Small Speculum Pack is a package containing 10 individual Disposable, Single-use Spe |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PRO-FIT 90089473 not registered Live/Pending |
Pro Fit Technologies, LLC 2020-08-03 |
PRO-FIT 86799292 5261769 Live/Registered |
Electrostim Medical Services, Inc. 2015-10-26 |
PRO-FIT 86597846 not registered Dead/Abandoned |
Precision One Lifecare Limited 2015-04-15 |
PRO-FIT 86432613 4814688 Live/Registered |
KBK INDUSTRIES, LLC 2014-10-23 |
PRO-FIT 86376808 5091665 Live/Registered |
National Nail Corp. 2014-08-26 |
PRO-FIT 86088488 4676328 Live/Registered |
Conitex Sonoco USA Inc. 2013-10-10 |
PRO-FIT 86080194 4664627 Live/Registered |
Serta, Inc. 2013-10-01 |
PRO-FIT 85951948 not registered Dead/Abandoned |
Belkin International, Inc. 2013-06-05 |
PRO-FIT 85417480 not registered Dead/Abandoned |
DUMAN ALP 2011-09-08 |
PRO-FIT 85246634 4321466 Live/Registered |
TEXTRON INNOVATIONS INC. 2011-02-18 |
PRO-FIT 85188191 not registered Dead/Abandoned |
Weaver Leather, LLC 2010-12-01 |
PRO-FIT 78865718 3208876 Dead/Cancelled |
Kramer, Joseph 2006-04-20 |