DUALX DUAL PORT HEMOSTATIC AGENT DELIVERY TUBE

GUDID B707FD193000

HEMOSTATIC AGENT DELIVERY TUBE

Amplify Surgical, Inc.

Orthopaedic implant inserter/extractor, reusable
Primary Device IDB707FD193000
NIH Device Record Key0c94a1bd-a6b9-46de-acfd-ed61203bb0c4
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUALX DUAL PORT HEMOSTATIC AGENT DELIVERY TUBE
Version Model NumberFD19-30
Company DUNS081021000
Company NameAmplify Surgical, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com
Phone7652675439
Emailudi@amplifysurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB707FD193000 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MAXIntervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


[B707FD193000]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-29
Device Publish Date2022-03-21

Devices Manufactured by Amplify Surgical, Inc.

B707125355860 - DUALX DUAL PORT HEMOSTATIC AGENT DELIVERY TUBE (USA)2025-06-06 HEMOSTATIC AGENT DELIVERY TUBE US MANUFACTURE
B70712535588001US0 - DUALX DUAL PORT CANNULA 30MM2025-06-06 30MM US MANUFACTURE
B70712535588002US0 - DUALX DUAL PORT CANNULA 40MM2025-06-06 40MM US MANUFACTURE
B70712535588003US0 - DUALX DUAL PORT CANNULA 50MM2025-06-06 50MM US MANUFACTURE
B70712535588004US0 - DUALX DUAL PORT CANNULA 60MM2025-06-06 60MM US MANUFACTURE
B70712535588005US0 - DUALX DUAL PORT CANNULA 70MM2025-06-06 70MM US MANUFACTURE
B70712535588006US0 - DUALX DUAL PORTAL CANNULA 80MM2025-06-06 80MM US MANUFACTURE
B70712535588007US0 - DUALX DUAL PORTAL CANNULA 90MM2025-06-06 90MM US MANUFACTURE

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