Oscar 2, Model 250D

GUDID 10840935108429

SUNTECH MEDICAL, INC.

Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder Blood pressure ambulatory recorder
Primary Device ID10840935108429
NIH Device Record Key67110625-8909-458b-ab05-332898a44ef0
Commercial Distribution StatusIn Commercial Distribution
Brand NameOscar 2, Model 250D
Version Model Number99-0233-00
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 Batchfalse
Serial Numbertrue
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

Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com
Phone919-654-2300
EmailUDI_Mail@suntechmed.com

Device Identifiers

Device Issuing AgencyDevice ID
GS110840935108429 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DXNSystem, Measurement, Blood-Pressure, Non-Invasive

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-11-08
Device Publish Date2019-04-06

On-Brand Devices [Oscar 2, Model 250D]

1084093510849899-0233-07
1084093510848199-0233-06
1084093510847499-0233-05
1084093510846799-0233-04
1084093510845099-0233-03
1084093510844399-0223-02
1084093510843699-0233-01
1084093510842999-0233-00

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