Revo Medical

Primary DI
00850035252314
Brand
Revo Medical
Company
Revo Medical Products Inc
Model
RM1797
Device description
ASTM Level 1 Procedure Mask, Earloop, Yellow
Published
2021-12-15
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
FXXMask, Surgical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FXXMask, SurgicalGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00850035252314PackageGS110In Commercial Distribution
00850035252192PrimaryGS10
00850035252093Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850035252314008500352523148500352523140850035252314
00850035252192008500352521928500352521920850035252192
00850035252093008500352520938500352520930850035252093

GMDN Terms#

Term, Definition table
TermDefinition
Surgical/medical face mask, single-useA flexible, loose-fitting mask designed to be placed over the mouth and/or nose of a healthcare worker to permit normal breathing while protecting the patient and wearer from the transfer of large particles (e.g., blood, body fluids, and airborne particulate materials) during medical procedures and patient examination; it is not a form-shaped filtering device (i.e., not a respirator). It is made of a flexible, porous fabric or paper material and is typically secured using elastic head straps or ties; it may incorporate a forming nosepiece (metal wire) and/or transparent face/eye visor intended to protect the upper face/eyes from debris/fluid. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in cool, dry, and well ventilated space out of direct sunlight

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
118289620
Device count
50
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
true
Expiration date on label
false
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850035252116Revo MedicalRM17882021-12-15
00850035252123Revo MedicalRM17892021-12-15
00850035252130Revo MedicalRM17902021-12-15
00850035252147Revo MedicalRM17912021-12-15
00850035252154Revo MedicalRM17922021-12-15
00850035252161Revo MedicalRM17942021-12-15
00850035252192Revo MedicalRM17972021-12-15
00850035252208Revo MedicalRM17982021-12-15
00850035252215Revo MedicalRM17932021-12-15
00850035252000Revo MedicalRM17882021-12-15
00850035252239Revo MedicalRM17892021-12-15
00850035252024Revo MedicalRM17902021-12-15
00850035252253Revo MedicalRM17912021-12-15
00850035252260Revo MedicalRM17922021-12-15
00850035252284Revo MedicalRM17942021-12-15
00850035252321Revo MedicalRM17982021-12-15
00850035252277Revo MedicalRM17932021-12-15

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Primary DI, Brand, Company table
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