ProLife

GUDID 10840935110262

SUNTECH MEDICAL, INC.

Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable Blood pressure cuff, reusable
Primary Device ID10840935110262
NIH Device Record Keyc0c7f27c-fab6-4568-879d-5ad7843cc7eb
Commercial Distribution StatusIn Commercial Distribution
Brand NameProLife
Version Model Number98-040J-08
Company DUNS148191133
Company NameSUNTECH MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com
Phone+1-919-654-2300
EmailUDI_mail@suntechmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110840935110262 [Primary]

FDA Product Code

DXQBlood Pressure Cuff

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-19
Device Publish Date2023-06-09

On-Brand Devices [ProLife]

1084093511026298-040J-08
1084093511025598-040H-08
1084093511024898-040G-08
1084093511023198-040F-08
1084093511021798-040E-08

Trademark Results [ProLife]

Mark Image

Registration | Serial
Company
Trademark
Application Date
PROLIFE
PROLIFE
98236494 not registered Live/Pending
PERSONA COMERCIO, IMPORTACAO E EXPORTACAO LTDA
2023-10-23
PROLIFE
PROLIFE
88894657 not registered Live/Pending
Shenzhen Hongyunda Electronic Technology Co., Ltd.
2020-04-30
PROLIFE
PROLIFE
81036660 1036660 Dead/Cancelled
J. Capps & Sons, Limited
0000-00-00
PROLIFE
PROLIFE
79123161 4464419 Live/Registered
ZOODIACO
2012-10-08
PROLIFE
PROLIFE
75268514 not registered Dead/Abandoned
LifeTech Industries, Ltd.
1997-04-03
PROLIFE
PROLIFE
74350366 not registered Dead/Abandoned
LifeTech Industries, Ltd.
1993-01-19
PROLIFE
PROLIFE
73458728 1354899 Dead/Cancelled
HEALTH SCIENCE CENTER, INC.
1983-12-27

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