FDA.reportPublic FDA data

Bemis

Primary DI
20073088149163
Brand
Bemis
Company
BEMIS MANUFACTURING COMPANY
Model
1500
Catalog number
1500 01; 1500 10
Device description
1500CC REUSABLE OUTER CANISTER WITH YELLOW BRACKET FOR QUICK-FIT LINER SYSTEM
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
false

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
10073088149166PackageGS11In Commercial Distribution
20073088149163PackageGS110In Commercial Distribution
00073088149169PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1007308814916610073088149166
2007308814916320073088149163
00073088149169000730881491690730881491690073088149169

GMDN Terms#

Term, Definition table
TermDefinition
Surgical suction system collection container, reusableA 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 reusable device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Total Volume1500Milliliter

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
006072078
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
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

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
Primary DIBrandCompanyProduct codePublished
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14026704937278PLEUR-EVACTELEFLEX INCORPORATEDKDQ2026-05-08
14026704937285PLEUR-EVACTELEFLEX INCORPORATEDKDQ2026-05-08
14026704937292PLEUR-EVACTELEFLEX INCORPORATEDKDQ2026-05-08
14026704937353PLEUR-EVACTELEFLEX INCORPORATEDKDQ2026-05-08
00628725095363Pleural Drain Dry Seal System CHS USA Inc.KDQ2026-04-17
00628725095370Pleural Drain Wet Seal System CHS USA Inc.KDQ2026-04-17
40884389968100MEDLINEMEDLINE INDUSTRIES, INC.KDQ2026-01-29
40884389968124MEDLINEMEDLINE INDUSTRIES, INC.KDQ2026-01-29
40888277143020MEDLINEMEDLINE INDUSTRIES, INC.KDQ2026-01-29
40888277143518MEDLINEMEDLINE INDUSTRIES, INC.KDQ2026-01-29
40884389968070MEDLINEMEDLINE INDUSTRIES, INC.KDQ2025-11-28
14026704912190PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-09-17
14026704911780PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-09-04
14026704911902PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-07-02
14026704911872PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911889PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911896PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911919PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911926PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911933PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
14026704911940PLEUR-EVACTELEFLEX INCORPORATEDKDQ2025-03-12
10192253002652Thora-SealCardinal Health 200, LLCKDQ2025-02-19
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