Mobi-C MB943R

GUDID 03662663000376

LDR Spine Usa, Inc.

Surgical implant template, reusable
Primary Device ID03662663000376
NIH Device Record Key78140f25-505f-4647-99e7-84628451e9cb
Commercial Distribution StatusIn Commercial Distribution
Brand NameMobi-C
Version Model NumberMB943R
Catalog NumberMB943R
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 Dimensions

Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter
Width15 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS103662663000376 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


[03662663000376]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2022-03-10
Device Publish Date2018-12-13

On-Brand Devices [Mobi-C]

03662663002097MOBI-C IMPLANT M « STANDARD » 19x19 H7 US
03662663002080MOBI-C IMPLANT M « STANDARD » 19x19 H6 US
03662663002073MOBI-C IMPLANT M « STANDARD » 19x19 H5 US
03662663002066MOBI-C IMPLANT M « STANDARD » 17x19 H7 US
03662663002059MOBI-C IMPLANT M « STANDARD » 17x19 H6 US
03662663002042MOBI-C IMPLANT M « STANDARD » 17x19 H5 US
03662663002035MOBI-C IMPLANT M « STANDARD » 17x17 H7 US
03662663002028MOBI-C IMPLANT M « STANDARD » 17x17 H6 US
03662663002011MOBI-C IMPLANT M « STANDARD » 17x17 H5 US
03662663000253MB917R
03662663000437MB949R
03662663000420MB948R
03662663000413MB947R
03662663000406MB946R
03662663000390MB945R
03662663000383MB944R
03662663000376MB943R
03662663000369MB942R
03662663000246MB906R
03662663000239MB904R
03662663000222MB903R
03662663000215MB900R

Trademark Results [Mobi-C]

Mark Image

Registration | Serial
Company
Trademark
Application Date
MOBI-C
MOBI-C
78514826 3197424 Live/Registered
LDR MEDICAL, S.A.S.
2004-11-10

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