EMESIS BASIN ST8

GUDID 00192896095045

EMESIS BASIN

SONTEC INSTRUMENTS, INC.

Emesis bowl, reusable
Primary Device ID00192896095045
NIH Device Record Key0012d659-c323-4696-94b4-d550f64c23ed
Commercial Distribution StatusIn Commercial Distribution
Brand NameEMESIS BASIN
Version Model NumberST8
Catalog NumberST8
Company DUNS040729840
Company NameSONTEC INSTRUMENTS, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Datefalse
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(800) 821-7496
Emailinfo@sontecinstruments.com

Device Dimensions

Total Volume12 Fluid Ounce

Device Identifiers

Device Issuing AgencyDevice ID
GS100192896095045 [Primary]

FDA Product Code

FNYBASIN, EMESIS

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00192896095045]

Moist Heat or Steam Sterilization;Dry Heat Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-03-15
Device Publish Date2019-03-07

On-Brand Devices [EMESIS BASIN]

00192896070615EMESIS BASIN
00192896095045EMESIS BASIN
00192896105362Emesis Basin 10 Ounces

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