FDA.reportPublic FDA data

Buffalo Filter

Primary DI
10851136002669
Brand
Buffalo Filter
Company
Buffalo Filter
Model
BILF101
Device description
Laser & Electrosurgery In-Line Filter
Published
2017-01-13
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
FYDApparatus, Exhaust, Surgical

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
FYDApparatus, Exhaust, SurgicalGeneral, Plastic Surgery2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10851136002669PackageGS110Not in Commercial Distribution
00851136002662PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085113600266910851136002669
00851136002662008511360026628511360026620851136002662

GMDN Terms#

Term, Definition table
TermDefinition
Suction system filter, plume particulateA screening device installed within the suction tubing line of a suction system, or the suction tubing used with a central vacuum system, to extract particulates from the plume of smoke created typically through the use of various tissue-burning surgical devices (e.g., laser, electrosurgical diathermy device), to prevent clogging of the suction or vacuum system. It will typically have a hydrophobic membrane that retains the particulate/bacterial pathogens through a combination of mechanical, electrostatic, or other means. The device comes in various sizes and designs and can be made of translucent plastic, allowing for inspection when in use. This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Pore Size0.1Micrometer

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
716-835-7000bf.smoke.info@buffalofilter.com

Regulatory Flags#

DUNS number
787855907
Device count
1
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
00815198011031Buffalo FilterVT106102016-10-05
00815198011055Buffalo FilterVTWT4062016-09-30
00815198011086Buffalo FilterVT104052016-09-30
00815198011284Buffalo FilterVTWT2062016-09-30
00815198012519PenAdaptPA2010BCB2016-09-23
00815198012663Buffalo Filter777-007A2016-10-05
00815198012717InvuityPB1SEPB1SE2018-07-12
00815198012762OR-VACSEOOLLAP122018-07-12
00815198012779OR-VACOL3MT24OL3MT242018-07-12
00851136002068Buffalo FilterVTWT6242016-09-30
00851136002105Buffalo FilterVTWT4242016-09-30
00851136002143PenAdaptPA20102016-09-23
00851136002150Buffalo FilterVT103242016-10-05
00851136002174Buffalo FilterVT104242016-09-30
00851136002228PenAdaptPA2010CB2016-09-23
00851136002235Buffalo FilterVTVIC102016-09-30
00851136002266Buffalo FilterVT106242016-09-30
00851136002334Buffalo FilterPSFTS05PSFTS052017-01-06
00851136002358Buffalo FilterRF102102016-09-30
00851136002372PenAdaptPA1025CBPA1025CB2016-09-23

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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10840113242792BovieASPEN SURGICAL PRODUCTS, INC.FYD2026-09-18
30845854655492PlumeSafe® X5™Conmed CorporationFYD2026-07-23
10705036046523MegadyneETHICON ENDO-SURGERY, LLCFYD2026-05-27
10860012888808Flamingo Funnel (miniSQUAIR) - LargeNASCENT SURGICAL, LLCFYD2026-05-01
10860012888815Flamingo Funnel (microSQUAIR) - MediumNASCENT SURGICAL, LLCFYD2026-05-01
10860012888822Flamingo Funnel (nanoSQUAIR) - Small NASCENT SURGICAL, LLCFYD2026-05-01
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