Primary Device ID | 13700773727671 |
NIH Device Record Key | 28d91e0c-0c47-4054-8ce0-affbfac859cf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EXTERNAL OCULID MEDIUM BROWN® - 0,8 g |
Version Model Number | S3.60083 |
Company DUNS | 763408366 |
Company Name | FCI S A S FCI 20 22 |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 13700773727671 [Primary] |
MML | Weights, Eyelid, External |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-03-16 |
Device Publish Date | 2022-03-08 |
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13700773728081 - EZYPOR® Ø 16 mm | 2024-07-01 Orbital implant |
13700773728852 - EZYPOR® Ø 12 mm | 2024-07-01 Orbital implant |
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13700773735096 - OPHTACATH® 2 mm Unilateral Kit | 2024-01-05 A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic |
13700773735102 - OPHTACATH® 2 mm Bilateral Kit | 2024-01-05 A collection of various ophthalmic surgical instruments and the necessary materials intended to be used to perform an ophthalmic |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
EXTERNAL OCULID MEDIUM BROWN 79323722 not registered Live/Pending |
FRANCE CHIRURGIE INSTRUMENTATION SAS 2021-08-31 |