FDA.reportPublic FDA data

Insufflation Filter & Tubing Set w/ORing Quick Connector

Primary DI
B354OSITLQ0
Brand
Insufflation Filter & Tubing Set w/ORing Quick Connector
Company
ORANGE SURGICAL INSTRUMENTS, LLC
Model
OSITLQ
Device description
Insufflation Filter & Tubing Set w/O-Ring Quick Connector
Published
2016-11-15
Public version status
Update
Distribution status
Not in Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GEIElectrosurgical, Cutting & Coagulation & Accessories
HIFInsufflator, Laparoscopic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GEIElectrosurgical, Cutting & Coagulation & AccessoriesGeneral, Plastic Surgery2
HIFInsufflator, LaparoscopicObstetrics/Gynecology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K101733000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K101733000REUSABLE, DISPOSABLE LAPAROSCOPIC INSTRUMENT AND SURGICAL DEVICE AND ACCESSORIESSac, LLC Dba Pinnacle Medical Surgical2011-06-06GCJ

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
B354OSITLQ10PackageHIBCC10Not in Commercial Distribution
B354OSITLQ0PrimaryHIBCC0

GMDN Terms#

Term, Definition table
TermDefinition
Insufflation gas conditioning tubing setA collection of sterile and non-sterile devices intended to be used with an insufflation gas conditioning system and/or a laparoscopic gas distention system, or other gas source, to condition the insufflation gas stream [typically carbon dioxide (CO2)] by heating and humidifying it before introduction into the peritoneal cavity or a wound during laparoscopic or open surgery. It is available in various configurations but typically includes a connection tube for connection to the gas source, an electrically-heated tube for transport of the conditioned gas to the operative site, a humidification chamber, a gas filter, and connectors. This is a single-use device.

Regulatory Flags#

DUNS number
047063695
Device count
1
Lot or batch
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
B354OSRP80Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP81Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP82Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP83Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP84Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP85Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B354OSRP89Retrieval Pouch (Multi Deploy) 8 mmOSRP82026-07-29
B3543000011ThoraClear Y Connector3000-012025-11-25
B3543000012ThoraClear Y Connector3000-012025-11-25
B3543000013ThoraClear Y Connector3000-012025-11-25
B3543000014ThoraClear Y Connector3000-012025-11-25
B3543000015ThoraClear Y Connector3000-012025-11-25
B3543000019ThoraClear Y Connector3000-012025-11-25
B3543000010ThoraClear Y Connector3000-012025-11-25
B354OS3CDBK23 Ring Suture Passer - BariatricOS3CDBK2023-07-07
B354OS3CDBK33 Ring Suture Passer - BariatricOS3CDBK2023-07-07
B3541011Duck Bill Forceps Inner Shaft 10mm1012023-07-19
B3541012Duck Bill Forceps Inner Shaft 10mm1012023-07-19
B3541013Duck Bill Forceps Inner Shaft 10mm1012023-07-19
B3541014Duck Bill Forceps Inner Shaft 10mm1012023-07-19

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Primary DI, Brand, Company table
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00724995269586Snowden-PencerSTERIS Deutschland GmbHGEI2026-09-25
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10840113236852BovieASPEN SURGICAL PRODUCTS, INC.GEI2026-09-21
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