Mobi-C Plug & Fit MB9074R

GUDID 03662663001458

LDR Spine Usa, Inc.

Bone distraction forceps
Primary Device ID03662663001458
NIH Device Record Key7e07a598-8ec7-4536-826e-eb3ba86a9d0b
Commercial Distribution StatusIn Commercial Distribution
Brand NameMobi-C Plug & Fit
Version Model NumberMB9074R
Catalog NumberMB9074R
Company DUNS615789729
Company NameLDR Spine Usa, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
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 Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com
Phone800-699-3360
Emailcustserv@ldrspine.com

Device Identifiers

Device Issuing AgencyDevice ID
GS103662663001458 [Primary]

FDA Product Code

GENForceps, General & Plastic Surgery

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


[03662663001458]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2022-03-10
Device Publish Date2018-12-12

On-Brand Devices [Mobi-C Plug & Fit]

03662663001465MB9075R
03662663046183MB992
03662663032896MB992-G
03662663002561MB991
03662663001458MB9074R
03662663001441MB9073R
03662663001434MB9072R

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.