Primary Device ID | 53760087120252 |
NIH Device Record Key | 3b676a1a-e26e-4597-a6f6-dcf069a011e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Surgical depth gauge, single-use |
Version Model Number | SIZER FOR SELF-RETAINING BICANALICULUS INTUBATION |
Catalog Number | S1.1289U |
Company DUNS | 763408366 |
Company Name | FCI S A S FCI 20 22 |
Device Count | 5 |
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 | true |
Manufacturing Date | true |
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 | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com | |
Phone | 800-932-4202 |
orders@fci-ophthalmics.com |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Length | 80 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 03760087120257 [Primary] |
GS1 | 53760087120252 [Unit of Use] |
HNL | Probe, Lachrymal |
Steralize Prior To Use | true |
Device Is Sterile | true |
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
[53760087120252]
Ethylene Oxide
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-03-16 |
Device Publish Date | 2020-03-06 |
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