Disposable cuff

GUDID 20840935107603

SUNTECH MEDICAL, INC.

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Primary Device ID20840935107603
NIH Device Record Key8d4b10d9-8fb0-4a42-8afe-6601c7281c47
Commercial Distribution StatusIn Commercial Distribution
Brand NameDisposable cuff
Version Model Number98-0399-C3
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com
Phone1-919-654-2300
EmailUDI_MAIL@suntechmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110840935107606 [Primary]
GS120840935107603 [Package]
Contains: 10840935107606
Package: Box [5 Units]
In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXQBlood Pressure Cuff

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-07-22
Device Publish Date2017-05-25

On-Brand Devices [Disposable cuff]

1084093510637198-0399-26
1084093510612898-0399-56
1084093510611198-0399-57
1084093510513898-0799-17
1084093510508498-0799-07
1084093510423098-0799-87
1084093510384498-0399-A6
1084093510375297-1108-03
1084093510368498-0799-86
1084093510363998-0399-D7
1084093510362298-0399-D6
1084093510314198-0399-37
1084093510313498-0399-36
1084093510236698-0799-77
1084093510230498-0799-76
1084093510085098-0399-G6
1084093510084398-0399-G7
1084093510065298-0799-47
1084093510064598-0799-46
1084093510051598-0799-37
1084093510049298-0799-36
1084093510033198-0799-27
1084093510031798-0799-26
1084093510007298-0799-16
1084093510002798-0799-06
2084093510765898-0399-C8
1084093510636498-0399-28
1084093510626598-0400-38
1084093510608198-0399-58
1084093510424798-0799-88
1084093510364698-0399-D8
1084093510239798-0799-78
1084093510080598-0399-A8
1084093510078298-0399-G8
1084093510066998-0799-48
1084093510053998-0799-38
1084093510034898-0799-28
1084093510032498-0399-78
1084093510011998-0799-18
1084093510003498-0799-08
2084093510840297-1108-12
2084093510839697-1108-11
2084093510838997-1108-10
2084093510837297-1108-09
2084093510821198-0399-7K
2084093510820498-0399-5K
2084093510819898-0399-2K
2084093510818198-0399-1K
2084093510817498-0399-0K
2084093510816798-0799-6K

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