Hemolung® Cartridge with Blood Tubing

GUDID 00850046004254

Hemolung® Cartridge with Blood Tubing

Alung Technologies, Inc.

Mobile extracorporeal gas exchange system
Primary Device ID00850046004254
NIH Device Record Keya2165698-dd2a-46c8-835d-4411d39cec7d
Commercial Distribution StatusIn Commercial Distribution
Brand NameHemolung® Cartridge with Blood Tubing
Version Model Number40400
Company DUNS129408592
Company NameAlung Technologies, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com
Phone(412) 697-3370
Emailtl.regulatory@livanova.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850046004254 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

QOHExtracorporeal System For Carbon Dioxide Removal

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-03-01
Device Publish Date2023-02-21

Devices Manufactured by Alung Technologies, Inc.

00850046004056 - Hemolung® CR4 Controller2023-03-01 Hemolung® CR4 Controller
00850046004223 - Hemolung® Cartridge Kit2023-03-01 Hemolung® Cartridge Kit
00850046004230 - Hemolung® Accessories Kit2023-03-01 Hemolung® Accessories Kit
00850046004247 - Hemolung® Rinse Back Kit2023-03-01 Hemolung® Rinse Back Kit
00850046004254 - Hemolung® Cartridge with Blood Tubing2023-03-01Hemolung® Cartridge with Blood Tubing
00850046004254 - Hemolung® Cartridge with Blood Tubing2023-03-01 Hemolung® Cartridge with Blood Tubing
00850046004278 - Hemolung® 15.5 Fr Femoral Catheter Kit2023-03-01 Hemolung® 15.5 Fr Femoral Catheter Kit
00850046004308 - Hemolung® 15.5 Fr Jugular Catheter Kit2023-03-01 Hemolung® 15.5 Fr Jugular Catheter Kit
00850046004322 - Hemolung® Catheter Spare Parts Kit2023-03-01 Hemolung® Catheter Spare Parts Kit

Trademark Results [Hemolung]

Mark Image

Registration | Serial
Company
Trademark
Application Date
HEMOLUNG
HEMOLUNG
97051104 not registered Live/Pending
ALung Technologies, Inc.
2021-09-29
HEMOLUNG
HEMOLUNG
77694732 3911641 Live/Registered
ALung Technologies, Inc.
2009-03-19

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