Insufflator Filter Assembly

Primary DI
00850082007196
Brand
Insufflator Filter Assembly
Company
ARMM INC.
Model
21002
Device description
Insufflator Filter Assembly - Rotating Male Luer / Multiple Barb
Published
2023-06-08
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
HIFInsufflator, Laparoscopic

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
HIFInsufflator, LaparoscopicObstetrics/Gynecology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10850082007193PrimaryGS10
00850082007196Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085008200719310850082007193
00850082007196008500820071968500820071960850082007196

GMDN Terms#

Term, Definition table
TermDefinition
Endoscopic insufflation tubing set, single-useA collection of flexible tubing intended to channel medical gas [e.g., carbon dioxide (CO2), medical air] from its source into a body cavity for insufflation during endoscopy (e.g., gastrointestinal endoscopy, laparoscopy, arthroscopy). It includes synthetic polymer tubing and associated connectors; it may in addition be intended for endoscopic lens drying, and may include additional tubing for delivery of a sterile irrigation solution for endoscopic irrigation. This is a single-use device.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
7148488190info@armminc.com

Regulatory Flags#

DUNS number
797391778
Device count
10
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
true
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
10850082007384MedDrain232142017-02-22
10850082007391MedDrain232162017-02-22
10850082007407MedDrain232202017-02-22
10850082007414MedDrain232242017-02-22
10850082007421MedDrain232282017-02-22
10850082007438MedDrain232322017-02-22
10850082007445MedDrain232362017-02-22
10850082007452MedDrain232402017-02-22
10850082007469MedDrain23214C2017-02-22
10850082007476MedDrain23216C2017-02-22
10850082007483MedDrain23220C2017-02-22
10850082007490MedDrain23224C2017-02-22
10850082007506MedDrain23228C2017-02-22
10850082007513MedDrain23232C2017-02-22
10850082007520MedDrain23236C2017-02-22
10850082007537MedDrain23240C2017-02-22
10850082007544MedDrain2320162017-02-23
10850082007551MedDrain2320202017-02-23
10850082007568MedDrain2320242017-02-23
10850082007575MedDrain2320282017-02-23

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Primary DI, Brand, Company table
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B3543000014ThoraClear Y ConnectorORANGE SURGICAL INSTRUMENTS, LLCHIF2025-11-25
B3543000015ThoraClear Y ConnectorORANGE SURGICAL INSTRUMENTS, LLCHIF2025-11-25
B3543000019ThoraClear Y ConnectorORANGE SURGICAL INSTRUMENTS, LLCHIF2025-11-25
B3543000010ThoraClear Y ConnectorORANGE SURGICAL INSTRUMENTS, LLCHIF2025-11-25
04046955813353AESCULAPAesculap AGHIF2025-05-18
04953170467219HIGH FLOW INSUFFLATION UNITOLYMPUS MEDICAL SYSTEMS CORP.HIF2025-02-27
04055207007822NARichard Wolf GmbHHIF2024-08-19
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10845854045633AIRSEALConmed CorporationHIF2024-03-27
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10845854045367CONMEDConmed CorporationHIF2023-12-04
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