Primary Device ID | 10871321001444 |
NIH Device Record Key | 1771e6dc-d9d1-4394-a5f4-72285eb6cb9b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Partial Thickness Sponge |
Version Model Number | S 1984-5 |
Company DUNS | 248911026 |
Company Name | Labtician Ophthalmics, Inc |
Device Count | 5 |
DM Exempt | false |
Pre-market Exempt | false |
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 | 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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00087132100280 [Unit of Use] |
GS1 | 00187132100287 [Unit of Use] |
GS1 | 10871321001444 [Primary] |
HQJ | Implant, Absorbable, (Scleral Buckling Methods) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-01-27 |
Device Publish Date | 2015-10-09 |
18713210001451 | S 1984-7.5 |
18713210001444 | S 1984-5 |
18713210001437 | S 1984-3.3 |
18713210001420 | S 1984-3 |
18713210001413 | S 1984-2.5 |
10871321001451 | S 1984-7.5 |
10871321001444 | S 1984-5 |
10871321001437 | S 1984-3.3 |
10871321001420 | S 1984-3 |
10871321001413 | S 1984-2.5 |