BEMIS

Primary DI
10073088149494
Brand
BEMIS
Company
BEMIS MANUFACTURING COMPANY
Model
3002 055
Catalog number
3002 055
Device description
3000CC HIFLOW SUCTION CANISTER WITH AEROSTAT FILTER, FLOAT VALVE SHUT OFF WITH GREEN LID
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
OTC
true
Single use
true

Product Codes#

Code, Name table
CodeName
KDQBottle, Collection, Vacuum

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KDQBottle, Collection, VacuumGeneral Hospital2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10073088149494PrimaryGS10
00073088149497Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1007308814949410073088149494
00073088149497000730881494970730881494970073088149497

GMDN Terms#

Term, Definition table
TermDefinition
Surgical suction system collection container, single-useA cylindrical or bottle-shaped sealable container intended to be used as a component of a surgical suction system to collect aspirated materials (e.g., blood/bodily fluids, gases, body tissues) from a surgical site for disposal (e.g., to prevent backflow) or diagnostic/therapeutic purposes (e.g., polyp trap). It may be used singularly or connected in a series to provide greater capacity, and may be graduated to facilitate determination of the quantity of its contents; it may also be used in conjunction with aspiration liners and may include lid, microbial/hydrophobic filters or tubing. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Total Volume3000Milliliter

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00KEEP AWAY FROM SUNLIGHT

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
006072078
Device count
36
Premarket exempt
true
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10073088161755Bemis7209824-J7209824-J2021-06-17
10073088165296BemisPAL-SC-3000PAL-SC-30002025-02-07
10073088165302BEMISPAL-SC-2000PAL-SC-20002025-02-07
00073088165299BemisPAL-SC-3000PAL-SC-30002025-02-07
00073088165305BEMISPAL-SC-2000PAL-SC-20002025-02-07
10073088150414Bemis5350105350102016-09-24
10073088150490Bemis5384105384102016-09-24
10073088162660BEMIS6354106354102024-11-25
00073088162663BEMIS6354106354102024-11-25
10073088162646BEMIS6244106244102024-10-23
00073088162649BEMIS6244106244102024-10-23
10073088162653BEMIS6344106344102024-10-15
10073088162677BEMIS6364106364102024-10-15
00073088162656BEMIS6344106344102024-10-15
00073088162670BEMIS6364106364102024-10-15
20073088150565BEMIS8002 055 N8002 055 N 2024-10-15
10073088150421Bemis5355105355102016-09-24
10073088150476Bemis5381105381102016-09-24
10073088150483Bemis5382105382102016-09-24
10073088164244BEMIS8002004L108002004L102024-05-17

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Primary DI, Brand, Company table
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14026704911919PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911926PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911933PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
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10192253002645Thora-SealCardinal Health 200, LLCKDQ2025-02-18
10192253002669Thora-SealCardinal Health 200, LLCKDQ2025-02-18
10192253002676ArgyleCardinal Health 200, LLCKDQ2025-02-18
10073088165296BemisBEMIS MANUFACTURING COMPANYKDQ2025-02-07
10073088165302BEMISBEMIS MANUFACTURING COMPANYKDQ2025-02-07