Primary Device ID | 03662663000413 |
NIH Device Record Key | 4986895e-9169-4a79-9ab4-d4af238a909e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Mobi-C |
Version Model Number | MB947R |
Catalog Number | MB947R |
Company DUNS | 615789729 |
Company Name | LDR Spine Usa, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com | |
Phone | 800-699-3360 |
custserv@ldrspine.com |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Width | 19 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03662663000413 [Primary] |
LXH | Orthopedic Manual Surgical Instrument |
Steralize Prior To Use | true |
Device Is Sterile | false |
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
[03662663000413]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-03-10 |
Device Publish Date | 2018-12-13 |
03662663002097 | MOBI-C IMPLANT M « STANDARD » 19x19 H7 US |
03662663002080 | MOBI-C IMPLANT M « STANDARD » 19x19 H6 US |
03662663002073 | MOBI-C IMPLANT M « STANDARD » 19x19 H5 US |
03662663002066 | MOBI-C IMPLANT M « STANDARD » 17x19 H7 US |
03662663002059 | MOBI-C IMPLANT M « STANDARD » 17x19 H6 US |
03662663002042 | MOBI-C IMPLANT M « STANDARD » 17x19 H5 US |
03662663002035 | MOBI-C IMPLANT M « STANDARD » 17x17 H7 US |
03662663002028 | MOBI-C IMPLANT M « STANDARD » 17x17 H6 US |
03662663002011 | MOBI-C IMPLANT M « STANDARD » 17x17 H5 US |
03662663000253 | MB917R |
03662663000437 | MB949R |
03662663000420 | MB948R |
03662663000413 | MB947R |
03662663000406 | MB946R |
03662663000390 | MB945R |
03662663000383 | MB944R |
03662663000376 | MB943R |
03662663000369 | MB942R |
03662663000246 | MB906R |
03662663000239 | MB904R |
03662663000222 | MB903R |
03662663000215 | MB900R |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MOBI-C 78514826 3197424 Live/Registered |
LDR MEDICAL, S.A.S. 2004-11-10 |