Primary Device ID | 00854066006137 |
NIH Device Record Key | 56d47d14-3991-4406-ad13-e4a8010de089 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | I00041 |
Company DUNS | 859186348 |
Company Name | INTEGRATED ORBITAL IMPLANTS 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 | true |
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 | 1-800-424-6537 |
haimplants@ioi.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00854066006137 [Primary] |
HQN | Conformer, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00854066006137]
Hydrogen Peroxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2015-12-01 |
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00854066006014 - Bio-Eye® | 2018-07-06 Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |
00854066006021 - Bio-Eye® | 2018-07-06 Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |
00854066006038 - Bio-Eye® | 2018-07-06 Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |
00854066006045 - Bio-Eye® | 2018-07-06 Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |
00854066006052 - Bio-Eye® | 2018-07-06 Coated Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |
00854066006069 - Bio-Eye® | 2018-07-06 Coated Hydroxyapatite (HA) Orbital Implant & Conformer used for enucleations and eviscerations. |