Insufflator Tubing Set with Filter

GUDID 10850082007131

Insufflator Tubing Set with Filter - 10' / Rotating Male Luers

ARMM INC.

Endoscopic insufflation tubing set, single-use
Primary Device ID10850082007131
NIH Device Record Keyecdae4ad-ccbf-474a-84c0-5a533828fc73
Commercial Distribution StatusIn Commercial Distribution
Brand NameInsufflator Tubing Set with Filter
Version Model Number21110
Company DUNS797391778
Company NameARMM INC.
Device Count10
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com
Phone7148488190
Emailinfo@armminc.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850082007134 [Unit of Use]
GS110850082007131 [Primary]

FDA Product Code

HIFInsufflator, Laparoscopic

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-05-10
Device Publish Date2016-09-06

Devices Manufactured by ARMM INC.

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