Primary Device ID | 10697660001095 |
NIH Device Record Key | f4811f17-2f82-4462-a1f2-8aa0bdb03a3d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Bilateral Conformer 18/20 Small |
Version Model Number | 19-102 |
Company DUNS | 257382580 |
Company Name | Oculo-Plastik Inc |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Safe |
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 | true |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 514-381-3292 |
sales@oculoplastik.com |
Depth | 4 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10697660001095 [Primary] |
HIBCC | M8721910207 [Previous] |
HQN | Conformer, Ophthalmic |
Steralize Prior To Use | true |
Device Is Sterile | false |
[10697660001095]
Hydrogen Peroxide;Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-29 |
Device Publish Date | 2019-10-21 |
10697660001095 | Conformers (made of acrylic or PMMA) are single use devices. They are used to keep the form of t |
M8721910207 | Conformers (made of acrylic or PMMA) are single use devices. They are used to keep the form of t |