Teeth Screw Driver

GUDID 04719872108795

A mechanical device without adjustable parts intended to be placed between the teeth of the upper and lower jaws of a patient to maintain an open oral cavity, typically during emergent placement of an artificial airway or for an oral surgical intervention.

ENTER MEDICAL CORPORATION

Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable Mouth gag, non-adjustable
Primary Device ID04719872108795
NIH Device Record Key9ab886ed-d2cc-43e5-95ce-d9da49a36e02
Commercial Distribution StatusIn Commercial Distribution
Brand NameTeeth Screw Driver
Version Model NumberPN-2002
Company DUNS658833116
Company NameENTER MEDICAL CORPORATION
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 Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104719872108795 [Primary]

FDA Product Code

KBWScrew, Oral

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-06-27
Device Publish Date2023-06-19

Devices Manufactured by ENTER MEDICAL CORPORATION

04719872100607 - RESERVOIR2023-10-27 RESERVOIR
04719872101208 - Seal Rite Mask2023-10-27 Seal Rite Mask
04719872102021 - Catheter Mount2023-10-27 Catheter Mount
04719872103028 - Bubble Humidifier2023-10-27 Bubble Humidifier
04719872104414 - Nasal Cannula2023-10-27 Nasal Cannula
04719872104568 - reusable resuscitator2023-10-27 reusable resuscitator
04719872109631 - Disposable Resuscitator2023-10-27 Disposable Resuscitator
04719872109853 - Anaesthetic Face Mask2023-10-27 Anaesthetic Face Mask

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