Disposable Cuff

GUDID 20840935109348

SUNTECH MEDICAL, INC.

Blood pressure cuff, reusable
Primary Device ID20840935109348
NIH Device Record Keyf9974769-2930-4a78-bd87-6c9bbb2c3b18
Commercial Distribution StatusIn Commercial Distribution
Brand NameDisposable Cuff
Version Model Number98-0500-97
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 Latextrue
RX Perscriptiontrue
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
GS110840935109341 [Primary]
GS120840935109348 [Package]
Contains: 10840935109341
Package: Box [20 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 StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-08-28
Device Publish Date2020-08-20

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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