DISCOVISC
GUDID 00380651837102
DISCOVISC 1.0ML
Alcon Laboratories, Inc.
Aqueous/vitreous humour replacement medium kit Primary Device ID 00380651837102 NIH Device Record Key 3766c46a-7e7f-494c-87a4-4c49edf194ec Commercial Distribution Status In Commercial Distribution Brand Name DISCOVISC Version Model Number 8065183710 Company DUNS 008018525 Company Name Alcon Laboratories, Inc. 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 false Expiration Date true Donation Id Number false Contains Natural Rubber Latex false Labeled No Natural Rubber Latex true RX Perscription true OTC Over-The-Counter false
Customer Support Contacts
Phone +1(800)-862-5266 Email web.masterus@alcon.com
Device Dimensions
Total Volume 1 Milliliter
Device Identifiers
Device Issuing Agency Device ID GS1 00380651837102 [Primary] GS1 20380651837106 [Package]
Package: CASE [85 Units]
In Commercial Distribution
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P840064
FDA Product Code
LZP Aid, Surgical, Viscoelastic
Sterilization
Steralize Prior To Use false Device Is Sterile true
Device Entry Metadata
Public Version Status Update Device Record Status Published Public Version Number 4 Public Version Date 2019-05-06 Device Publish Date 2015-03-31
Devices Manufactured by Alcon Laboratories, Inc.
10380657530660 - UNIPURE & UNIFEYE 2024-11-05 UNIPURE C3F8 Ophthalmic Gas in the UNIFEYE Gas Delivery System.
Intraocular Gas Delivery System intended to treat uncomplicated 10380657530677 - UNIPURE & UNIFEYE 2024-11-05 UNIPURE SF6 Ophthalmic Gas in the UNIFEYE Gas Delivery System.
Intraocular Gas Delivery System intended to treat uncomplicated 10380657530684 - UNIPURE & UNIPEXY 2024-11-05 UNIPURE C3F8 Ophthalmic Gas in the UNIPEXY Gas Delivery System.
Intraocular Gas Delivery System intended to treat uncomplicated 10380657530691 - UNIPURE & UNIPEXY 2024-11-05 UNIPURE SF6 Ophthalmic Gas in the UNIPEXY Gas Delivery System.
Intraocular Gas Delivery System intended to treat uncomplicated r 17612717072098 - FINESSE ModifEYE 2024-10-04 25G ModifEYE Soft Tip Backflush - Long 17612717072104 - FINESSE ModifEYE 2024-10-04 27+ ModifEYE Soft Tip Backflush - Long 17612717072067 - FINESSE ModifEYE 2024-10-03 25G ModifEYE Soft Tip Backflush 17612717072074 - FINESSE ModifEYE 2024-10-03 27+ ModifEYE Soft Tip Backflush
Trademark Results [DISCOVISC]
Mark Image
Registration | Serial Company Trademark
Application Date 
DISCOVISC 78404964 3038411 Live/RegisteredNOVARTIS AG 2004-04-20
Alcon Laboratories, Inc.
Aqueous/vitreous humour replacement medium kit| Primary Device ID | 00380651837102 |
| NIH Device Record Key | 3766c46a-7e7f-494c-87a4-4c49edf194ec |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | DISCOVISC |
| Version Model Number | 8065183710 |
| Company DUNS | 008018525 |
| Company Name | Alcon Laboratories, Inc. |
| 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 | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
| Phone | +1(800)-862-5266 |
| web.masterus@alcon.com |
Device Dimensions
| Total Volume | 1 Milliliter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00380651837102 [Primary] |
| GS1 | 20380651837106 [Package] Package: CASE [85 Units] In Commercial Distribution |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Approval: P840064
FDA Product Code
| LZP | Aid, Surgical, Viscoelastic |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-05-06 |
| Device Publish Date | 2015-03-31 |
Devices Manufactured by Alcon Laboratories, Inc.
| 10380657530660 - UNIPURE & UNIFEYE | 2024-11-05 UNIPURE C3F8 Ophthalmic Gas in the UNIFEYE Gas Delivery System. Intraocular Gas Delivery System intended to treat uncomplicated |
| 10380657530677 - UNIPURE & UNIFEYE | 2024-11-05 UNIPURE SF6 Ophthalmic Gas in the UNIFEYE Gas Delivery System. Intraocular Gas Delivery System intended to treat uncomplicated |
| 10380657530684 - UNIPURE & UNIPEXY | 2024-11-05 UNIPURE C3F8 Ophthalmic Gas in the UNIPEXY Gas Delivery System. Intraocular Gas Delivery System intended to treat uncomplicated |
| 10380657530691 - UNIPURE & UNIPEXY | 2024-11-05 UNIPURE SF6 Ophthalmic Gas in the UNIPEXY Gas Delivery System. Intraocular Gas Delivery System intended to treat uncomplicated r |
| 17612717072098 - FINESSE ModifEYE | 2024-10-04 25G ModifEYE Soft Tip Backflush - Long |
| 17612717072104 - FINESSE ModifEYE | 2024-10-04 27+ ModifEYE Soft Tip Backflush - Long |
| 17612717072067 - FINESSE ModifEYE | 2024-10-03 25G ModifEYE Soft Tip Backflush |
| 17612717072074 - FINESSE ModifEYE | 2024-10-03 27+ ModifEYE Soft Tip Backflush |
Trademark Results [DISCOVISC]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
DISCOVISC 78404964 3038411 Live/Registered |
NOVARTIS AG 2004-04-20 |
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