Primary Device ID | 08435389811473 |
NIH Device Record Key | 8d8e3bdb-d099-44c5-a9a3-040e449a5ef3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | INTERNA® WIDE IMPLANT CA D:5.5 L:11.5 |
Version Model Number | IIPACA5511 |
Company DUNS | 461665312 |
Company Name | BIOTECHNOLOGY INSTITUTE SL |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us | |
Phone | 2156464067 |
christinebattilana@bti-implant.us |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Length | 10 Millimeter |
Outer Diameter | 5 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08435389811473 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-06-12 |
Device Publish Date | 2018-09-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
INTERNA 79212490 5404000 Live/Registered |
INTERNA CONTRACT SPA 2017-04-14 |
INTERNA 76544837 2962844 Dead/Cancelled |
INTERNA CONTRACT S.P.A. 2003-09-12 |