Mirro-Vac Saliva Ejector Mirrors

Primary DI
00723896010013
Brand
Mirro-Vac Saliva Ejector Mirrors
Company
PRACTICON, INC.
Model
70-42615
Catalog number
70-42615
Device description
Reduce number of hands needed, instruments used and procedure time! The Mirro-Vac Saliva Ejector Mirror combines evacuator and mirror functions into one efficient instrument. Ideal for sealants, air abrasion, bonding and other dry field procedures. Upper suction inlet relieves tissue grab and ensures anti-fog acrylic mirror stays clear-even under direct exhalation. Size 4 lens with 35 degree inclination delivers standard mouth mirror feel and function without compromise. Easy-lift film protects mirror surface until use.Soft blue color eases patient anxiety.Round, knurled handle improves grip.Fully disposable, one-piece construction eliminates need for sterilization. 6" long. 50 mirrors per bag.
Published
2018-07-18
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Related Records

Product Codes

CodeName
EHZEvacuator, Oral Cavity

Product Code Classifications

CodeDeviceSpecialtyClass
EHZEvacuator, Oral CavityDental1

Identifiers And Packaging

IdentifierTypeAgencyPackage quantityStatus
00723896010013PackageGS120In Commercial Distribution
00723896010006PrimaryGS10
00723896001820Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifierGTIN-14 normalizedUPC-AEAN-13
00723896010013007238960100137238960100130723896010013
00723896010006007238960100067238960100060723896010006
00723896001820007238960018207238960018200723896001820

GMDN Terms

TermDefinition
Dental mirror, reusableA hand-held, dental instrument intended to be used by a dentist for intraoral inspection or inspection and retraction. It typically consists of a stainless steel shaft terminating at the distal end in a small round mirror that is angled to the shaft. This is a reusable device.

Sterilization Methods

Method

Regulatory Flags

DUNS number
119193803
Device count
50
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
false
Manufacturing date on label
false
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

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