Primary Device ID | H9813890770 |
NIH Device Record Key | 568d176f-a0b9-4c8e-9091-84ef963017b8 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ACF |
Version Model Number | 389.077 |
Catalog Number | 389077 |
Company DUNS | 832637081 |
Company Name | SYNTHES (U.S.A.) LP |
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 | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx | |
Phone | +1(800)255-2500 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10705034774343 [Primary] |
HIBCC | H9813890770 [Secondary] |
GDZ | HANDLE, SCALPEL |
Steralize Prior To Use | true |
Device Is Sterile | false |
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
[H9813890770]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-04-06 |
Device Publish Date | 2016-12-31 |
07611819738607 | ACF DETACHABLE TRIAL SPACER LORDOTIC 8MM |
07611819738584 | ACF DETACHABLE TRIAL SPACER LORDOTIC 6MM |
07611819738577 | ACF DETACHABLE TRIAL SPACER LORDOTIC 5MM |
07611819233911 | ACF TRIAL SPACER HANDLE |
07611819738744 | ACF DETACHABLE TRIAL SPACER CONVEX 10MM |
07611819738720 | ACF DETACHABLE TRIAL SPACER CONVEX 9MM |
07611819738706 | ACF DETACHABLE TRIAL SPACER CONVEX 8MM |
07611819738683 | ACF DETACHABLE TRIAL SPACER CONVEX 7MM |
07611819738652 | ACF DETACHABLE TRIAL SPACER CONVEX 6MM |
07611819738645 | ACF DETACHABLE TRIAL SPACER CONVEX 5MM |
07611819738638 | ACF DETACHABLE TRIAL SPACER LORDOTIC 10MM |
07611819738621 | ACF DETACHABLE TRIAL SPACER LORDOTIC 9MM |
07611819978157 | IMPLANT HOLDER FOR ACF ALLOGRAFT SPACERS |
H9813963840 | ACF SPACER IMPLANT HOLDER |
H9813890780 | SPN CORRECTION ACF EXTENDED IMPLANT HOLDER |
H9813890770 | SPN CORRECTION ACF TRIAL SPACER HANDLE |
07611819473119 | ACF HOLDER |
H9816900300 | ANTERIOR CERVICAL FUSION INSTRUMENT SET GRAPHIC CASE |
H9813048240 | ACF GRAPHIC CASE |