Primary Device ID | 00810027863119 |
NIH Device Record Key | 34ac81b6-22f0-43b0-be61-7e5c4c2741c7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | I3 Surgical Instruments |
Version Model Number | I3MMRP |
Company DUNS | 026108395 |
Company Name | I3 IMPLANT LLC |
Device Count | 1 |
DM Exempt | false |
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 | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00810027863119 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00810027863119]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-07-18 |
Device Publish Date | 2019-07-10 |
00810027863119 | I3MMRP |
00810027863102 | I3MMNP |
00810027863096 | I3SDB |
00810027863089 | I3SCD |
00810027863072 | I3DP199 |
00810027863065 | I3RTT |
00810027863058 | I3RR |
00810027863041 | I3PP16 |
00810027863034 | I3PP10 |
00810027863027 | I3HA15 |
00810027863010 | I3HA07 |
00810027863003 | I3TRP17 |
00810027862990 | I3TNP15 |
00810027862983 | I3PD15 |
00810027862976 | I3PD07 |
00810027862969 | I3HD15 |
00810027862952 | I3HD07 |
00810027862945 | I3IMM242 |
00810027862938 | I3PMM125 |
00810027862921 | I3D520 |
00810027862914 | I3D420 |
00810027862907 | I3D365 |
00810027862891 | I3D320 |
00810027862884 | I3D280 |
00810027862877 | I3DLCSET |
00810027862860 | I3DXT |
00810027862853 | I3MD19 |
00810027862846 | I3SK1 |
00810027863577 | I3SRP07 |
00810027863560 | I3SNP07 |